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characteristic: env biome

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tag: Namespace:PASTEUR INSTITUTE PARIS

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text: malaria parasite P. falciparum

characteristic: common name

text: Plasmodium falciparum 3D7

characteristic: description

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characteristic: organism

text: Plasmodium falciparum

characteristic: title


text: BI-UK

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text: Erythroid cell nuclearRNA Rep2

text: Mus musculus

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characteristic: tissue


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text: BI-UK

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text: BI-UK

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text: Mus musculus

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text: BI-UK

text: public

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text: Erythroid cell nuclearRNA Rep1

text: Mus musculus

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text: erythroid cells


text: fission yeast

characteristic: ArrayExpress-Species

characteristic: ArrayExpress-StrainOrLine

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:34Z-1446495

text: fission yeast

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text: fission yeast

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text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:14Z-1446573

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

characteristic: External Id

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text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:06Z-1446557

text: fission yeast

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text: fission yeast

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characteristic: INSDC center name

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:05Z-1446552

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:00Z-1446543

text: fission yeast

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text: Schizosaccharomyces pombe


text: fission yeast

text: SC

characteristic: INSDC last update

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:52Z-1446527

text: fission yeast

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text: fission yeast

text: SC

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characteristic: INSDC status

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:47Z-1446519

text: fission yeast

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text: Schizosaccharomyces pombe


text: fission yeast

text: SC

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characteristic: SRA accession

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:07Z-1446558

text: fission yeast

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text: fission yeast

text: SC

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:35Z-1446496

characteristic: Submitter Id

text: fission yeast

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text: Schizosaccharomyces pombe


text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:48Z-1446520

text: fission yeast

characteristic: common name

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:13Z-1446568

text: fission yeast

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text: Schizosaccharomyces pombe


text: fission yeast

text: SC

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:59Z-1446542

text: fission yeast

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text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:53Z-1446528

text: fission yeast

text: Schizosaccharomyces pombe

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text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:36Z-1446497

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:08Z-1446559

text: fission yeast

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text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:58Z-1446541

text: fission yeast

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text: Schizosaccharomyces pombe


text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:50Z-1446525

text: fission yeast

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text: fission yeast

text: SC

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:15Z-1446575

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:49Z-1446521

text: fission yeast

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text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:32Z-1446493

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:41Z-1446505

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:32Z-1446489

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:42Z-1446510

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:16Z-1446576

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:14Z-1446574

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:33Z-1446494

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:51Z-1446526

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:41Z-1446509

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:39Z-1446503

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:30Z-1446487

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:01Z-1446544

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:09Z-1446560

text: fission yeast

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text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:44Z-1446512

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:56Z-1446535

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:10Z-1446565

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:29Z-1446486

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:31Z-1446488

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:40Z-1446504

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:57Z-1446536

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:03Z-1446549

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:43Z-1446511

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:54Z-1446529

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:47Z-1446518

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:03Z-1446550

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:12Z-1446567

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:37Z-1446501

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:54Z-1446533

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:46Z-1446517

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:45Z-1446513

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:27Z-1446485

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:11Z-1446566

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:38Z-1446502

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:50:55Z-1446534

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


text: fission yeast

text: SC

text: public

text: Schizosaccharomyces_pombe-sc-2012-07-06T14:51:04Z-1446551

text: fission yeast

text: Schizosaccharomyces pombe

text: Schizosaccharomyces pombe


Focc

text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

text: BAH-GU

text: public

text: Focc

text: William Kirk and Ian Dublon

characteristic: collector

text: western flower thrips

characteristic: date

text: Greenhouse experiment, Keele University

characteristic: description

characteristic: genepoolID

characteristic: myid

text: Frankliniella occidentalis

text: Frankliniella occidentalis

text: RNAlater

characteristic: storage

text: Partial 454 transcriptome


Cpru

characteristic: ENA-FIRST-PUBLIC

text: SRA-Webin

text: BAH-GU

text: public

text: Cpru

text: nicola Sauvion and Gael Thebaud

text: plum psyllid

text: group A, plateau du Larzac, lieu dit Belvezet, France

text: Cacopsylla pruni

characteristic: organism

text: Cacopsylla pruni

text: RNAlater

text: Partial 454 transcriptome

characteristic: title


Msep

characteristic: ENA-LAST-UPDATE

text: SRA-Webin

characteristic: External Id

text: BAH-GU

characteristic: INSDC center name

text: public

text: Msep

text: Chris Simon

text: seventeen-year cicada

text: USA: Massachusetts. Mashpee.

text: Magicicada septendecim

text: Magicicada septendecim

text: 95% ethanol

text: Partial 454 transcriptome


Pspu

text: SRA-Webin

text: BAH-GU

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

text: Pspu

text: Joseph Hughes

text: meadow spittlebug

text: Field sample, University of Glasgow campus, UK

text: Philaenus spumarius

text: Philaenus spumarius

text: RNAlater

text: Partial 454 transcriptome


text: SRA-Webin

text: CAM-CEB

text: public

characteristic: SRA accession

characteristic: Submitter Id

text: cDNA produced from a cultured population of Adineta ricciae

text: Adineta ricciae

text: Adineta ricciae

text: cDNA from a population of A ricciae


text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

text: MPI-EVA

text: public

characteristic: anonymized name

text: human

characteristic: common name

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human37 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

characteristic: description

text: Homo sapiens

text: Homo sapiens

text: human26 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human43 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human48 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human21 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human18 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human13 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human17 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human3 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human32 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human8 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human49 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human38 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human20 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human4 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human14 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human34 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human29 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human44 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human39 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human33 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human40 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human25 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human1 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human9 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human30 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human5 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human24 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human19 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human15 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human28 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human41 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human10 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human35 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human45 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human47 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human6 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human12 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human22 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human2 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human27 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human42 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human50 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human46 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human36 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human16 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human7 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human11 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human31 DNA


text: SRA-Webin

text: MPI-EVA

text: public

text: human

text: DNA was aquired from CEPH-HGDP

text: Homo sapiens

text: Homo sapiens

text: human23 DNA


DCWC

text: SRA-Webin

text: UHOH

text: public

text: DCWC

text: Douglas-fir

text: 454 sequenced cDNA library of 17 individuals of three different provenances (Lowry Lake, Twin Harbors, Pend Oreille) of coastal Douglas-fir (Pseudotsuga menziesii). Stem tissue (wood) was extracted from 1.5 year old seedlings. The seedlings were well watered (control).

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii

text: Coastal Douglas-fir cDNA of stem tissue (wood) under control treatment


DCWS

text: SRA-Webin

text: UHOH

text: public

text: DCWS

text: Douglas-fir

text: 454 sequenced cDNA library of 14 individuals of three different provenances (Lowry Lake, Twin Harbors, Pend Oreille) of coastal Douglas-fir (Pseudotsuga menziesii). Stem tissue (wood) was extracted from 1.5 year old seedlings. The seedlings were severely water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DCNS

text: SRA-Webin

text: UHOH

text: public

text: DCNS

text: Douglas-fir

text: 454 sequenced cDNA library of 14 individuals of three different provenances (Lowry Lake, Twin Harbors, Pend Oreille) of coastal Douglas-fir (Pseudotsuga menziesii). Needle tissue was extracted from 1.5 year old seedlings. The seedlings were severely water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii

text: Coastal Douglas-fir cDNA of needle tissue under control treatment


DCWM

text: SRA-Webin

text: UHOH

text: public

text: DCWM

text: Douglas-fir

text: 454 sequenced cDNA library of 16 individuals of three different provenances (Lowry Lake, Twin Harbors, Pend Oreille) of coastal Douglas-fir (Pseudotsuga menziesii). Stem tissue (wood) was extracted from 1.5 year old seedlings. The seedlings were mildly water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DINS

text: SRA-Webin

text: UHOH

text: public

text: DINS

text: Douglas-fir

text: 454 sequenced cDNA library of 21 individuals of five different provenances (Fort Collins, Raton, Prince George, Salmon Arms, Twin Lake) of interior Douglas-fir (Pseudotsuga menziesii). Needle tissue was extracted from 1.5 year old seedlings. The seedlings were severely water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii

text: Interior Douglas-fir cDNA of needle tissue under control treatment


DIWC

text: SRA-Webin

text: UHOH

text: public

text: DIWC

text: Douglas-fir

text: 454 sequenced cDNA library of 20 individuals of five different provenances (Fort Collins, Raton, Prince George, Salmon Arms, Twin Lake) of interior Douglas-fir (Pseudotsuga menziesii). Stem tissue (wood) was extracted from 1.5 year old seedlings. The seedlings were well watered (control).

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii

text: Interior Douglas-fir cDNA of stem tissue (wood) under control treatment


DIWM

text: SRA-Webin

text: UHOH

text: public

text: DIWM

text: Douglas-fir

text: 454 sequenced cDNA library of 20 individuals of five different provenances (Fort Collins, Raton, Prince George, Salmon Arms, Twin Lake) of interior Douglas-fir (Pseudotsuga menziesii). Stem tissue (wood) was extracted from 1.5 year old seedlings. The seedlings were mildly water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DINC

text: SRA-Webin

text: UHOH

text: public

text: DINC

text: Douglas-fir

text: 454 sequenced cDNA library of 30 individuals of five different provenances (Fort Collins, Raton, Prince George, Salmon Arms, Twin Lake) of interior Douglas-fir (Pseudotsuga menziesii). Needle tissue was extracted from 1.5 year old seedlings. The seedlings were well watered (control).

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DCNC

text: SRA-Webin

text: UHOH

text: public

text: DCNC

text: Douglas-fir

text: 454 sequenced cDNA library of 17 individuals of three different provenances (Lowry Lake, Twin Harbors, Pend Oreille) of coastal Douglas-fir (Pseudotsuga menziesii). Needle tissue was extracted from 1.5 year old seedlings. The seedlings were well watered (control).

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DCNM

text: SRA-Webin

text: UHOH

text: public

text: DCNM

text: Douglas-fir

text: 454 sequenced cDNA library of 14 individuals of three different provenances (Lowry Lake, Twin Harbors, Pend Oreille) of coastal Douglas-fir (Pseudotsuga menziesii). Needle tissue was extracted from 1.5 year old seedlings. The seedlings were mildly water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DIWS

text: SRA-Webin

text: UHOH

text: public

text: DIWS

text: Douglas-fir

text: 454 sequenced cDNA library of 17 individuals of five different provenances (Fort Collins, Raton, Prince George, Salmon Arms, Twin Lake) of interior Douglas-fir (Pseudotsuga menziesii). Stem tissue (wood) was extracted from 1.5 year old seedlings. The seedlings were severely water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


DINM

text: SRA-Webin

text: UHOH

text: public

text: DINM

text: Douglas-fir

text: 454 sequenced cDNA library of 23 individuals of five different provenances (Fort Collins, Raton, Prince George, Salmon Arms, Twin Lake) of interior Douglas-fir (Pseudotsuga menziesii). Needle tissue was extracted from 1.5 year old seedlings. The seedlings were mildly water stressed.

text: Pseudotsuga menziesii

text: Pseudotsuga menziesii


text: SRA-Webin

text: EMBL

text: public

text: fruit fly

text: Drosophila melanogaster

text: Drosophila melanogaster

text: Oregon-R strain obtained from University of Zurich


text: SRA-Webin

text: EMBL

text: public

text: fruit fly

text: Drosophila melanogaster

text: Drosophila melanogaster

text: Canton-S strain obtained from Stanford University


text: SRA-Webin

text: EMBL

text: public

text: fruit fly

text: Drosophila melanogaster

text: Drosophila melanogaster

text: Oregon-R strain obtained from the European Molecular Biology Laboratory


CECEL LMG1612

text: SRA-Webin

text: VIB-UGENT

text: public

text: CECEL LMG1612

text: Cellulosimicrobium cellulans

text: Cellulosimicrobium cellulans

text: Cellulosimicrobium cellulans WGS


text: SRA-Webin

text: CRG

text: public

text: Megaselia abdita

text: Megaselia abdita

text: Megaselia abdita hiseq


text: SRA-Webin

text: CRG

text: public

text: Megaselia 454 transcriptome

text: Megaselia abdita

text: Megaselia abdita

text: Megaselia 454


text: SRA-Webin

text: CRG

text: public

text: mothmidge

text: Clogmia 454 transcriptome

text: Clogmia albipunctata

text: Clogmia albipunctata

text: Clogmia 454


text: SRA-Webin

text: CFENET-UBC

text: public

characteristic: collection date

text: HIV RNA from subject DS2 sera

text: Human immunodeficiency virus type 1 12-CRO

text: HIV-1 envelope glycoprotein (env) region C2-V3-C3


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS5 sera


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS1 sera


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS7 sera


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS4 sera


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS8 sera


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS6 sera


text: SRA-Webin

text: CFENET-UBC

text: public

text: HIV RNA from subject DS3 sera


Arabidopsis thaliana col-01

text: SRA-Webin

text: WUR

text: public

text: Arabidopsis thaliana col-01

text: thale cress

characteristic: ecotype

text: Arabidopsis thaliana

text: Arabidopsis thaliana

text: Leaf

characteristic: tissue type

text: Resequencing of Arabidopsis thaliana col-0


WGA Liriodendron tulipifera_18971

characteristic: ENA-FIRST-PUBLIC

text: SRA-Webin

text: WUR

text: public

text: WGA Liriodendron tulipifera_18971

text: J.W.C. Goedhart

characteristic: collected by

text: Hortus Leiden, the Netherlands

characteristic: geographic location (country and/or sea)

text: Liriodendron tulipifera

characteristic: organism

text: Liriodendron tulipifera

text: s.n.

characteristic: specimen voucher

text: Leaf

text: WGA of Liriodendron tulipifera_1897


Liriodendron tulipifera_fresh1

characteristic: ENA-LAST-UPDATE

text: SRA-Webin

characteristic: External Id

text: WUR

characteristic: INSDC center name

characteristic: INSDC first public

text: public

text: Liriodendron tulipifera_fresh1

text: Hortus, Leiden, the Netherlands

text: Liriodendron tulipifera

text: Liriodendron tulipifera

text: Leaf

text: WGS of Liriodendron tulipifera fresh leaf tissue

characteristic: title


WGS of Laburnum anagyroides_19461

text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

text: WUR

characteristic: INSDC last update

text: public

characteristic: INSDC status

characteristic: SRA accession

text: WGS of Laburnum anagyroides_19461

characteristic: Submitter Id

text: S.J. van Oostrom

text: Hortus Leiden, the Netherlands

text: Laburnum anagyroides

text: Laburnum anagyroides

text: s.n.

text: Herbarium tissue, leaf

text: WGS of Laburnum anagyroides_1946


name: WGS of Laburnum anagyoides fresh leaf tissue1

text: SRA-Webin

text: WUR

text: public

characteristic: collection date

text: Hortus Leiden, the Netherlands

text: Laburnum anagyroides

text: Laburnum anagyroides

text: Leaf


name: Resequencing of Agaricus bisporus herbarium specimen 9981733871

text: SRA-Webin

text: WUR

text: public

text: W. Kuys

text: Wissenkerke, Keihoogteweg, the Netherlands

text: Agaricus

text: Agaricus

text: Herbarium tissue, basidiome

characteristic: tissue type


name: Resequencing Pleurotus ostreatus herbarium specimen 9371582441

characteristic: ENA-FIRST-PUBLIC

text: SRA-Webin

text: WUR

text: public

text: M. Boetje-van Ruyven

text: oyster mushroom

characteristic: common name

text: Meyendel, the Netherlands

text: Pleurotus ostreatus

text: Pleurotus ostreatus

text: herbarium tissue, basidiome


name: Resequencing of Laccaria bicolor herbarium specimen 9902904191

text: SRA-Webin

text: WUR

text: public

text: E.C. Vellinga

characteristic: collected by

text: Roosendaal, De Moeren, the Netherlands

characteristic: geographic location (country and/or sea)

text: Laccaria

text: Laccaria

text: herbarium tissue, basidiome


name: Whole Genome Sequencing of Ceratitis capitata archived specimen 35_thorax_head

text: SRA-Webin

text: WUR

text: public

text: April 1995

text: Mediterranean fruit fly

characteristic: culture collection

text: Los Angeles, USA

text: Ceratitis capitata

characteristic: organism

text: Ceratitis capitata

text: archived specimen, thorax_head


name: Whole Genome Sequencing of Ceratitis capitata archived specimen 35_legs

characteristic: ENA-LAST-UPDATE

text: SRA-Webin

characteristic: External Id

text: WUR

text: public

text: April 1995

text: Mediterranean fruit fly

text: Los Angeles, USA

text: Ceratitis capitata

text: Ceratitis capitata

text: archived specimen, legs


name: Whole Genome Sequencing of Ceratitis capitata, fresh specimen, head and thorax

text: SRA-Webin

text: WUR

characteristic: INSDC center name

characteristic: INSDC first public

text: public

text: Vincenzo Girolami

text: Dec 2010

text: Mediterranean fruit fly

text: Sardinia, Italy

text: Ceratitis capitata

text: Ceratitis capitata

text: head and thorax


name: Whole Genome Sequencing of Ceratitis capitata, fresh specimen, legs

text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

text: WUR

text: public

text: Vincenzo Girolami

text: Dec 2010

text: Mediterranean fruit fly

text: Sardinia, Italy

text: Ceratitis capitata

text: Ceratitis capitata

text: legs

characteristic: title


name: Whole Genome Sequencing of Anoplophora glabripennis archived specimen1

text: SRA-Webin

text: WUR

characteristic: INSDC last update

text: public

characteristic: INSDC status

text: H. Stighter

text: July 1992

text: Asian longhorned beetle

text: s.n.

text: Beijing, China

text: Anoplophora glabripennis

text: Anoplophora glabripennis

text: archived specimen, 1 read leg


text: SRA-Webin

text: SYSU

text: public

characteristic: SRA accession

characteristic: Submitter Id

text: Neisseria gonorrhoeae

text: Neisseria gonorrhoeae


text: SRA-Webin

text: public

text: B17 zymodeme Tb rhodesiense

characteristic: description

text: Trypanosoma brucei rhodesiense

text: Trypanosoma brucei rhodesiense

text: B17 zymodeme Tb rhodesiense


characteristic: ENA-FIRST-PUBLIC

text: SRA-Webin

text: public

text: Z310 zymodeme Tb rhodesiense

text: Trypanosoma brucei rhodesiense

text: Trypanosoma brucei rhodesiense

text: Z310 zymodeme Tb rhodesiense


text: SRA-Webin

text: UNIFI

text: public

text: Whole Exome sequencing of melanoma cell lines

text: Homo

text: Homo

text: melanoma cell lines


text: SRA-Webin

text: UNIFI

text: public

text: Whole Exome sequencing of blood samples from healthy donors

text: Homo

text: Homo

text: blood samples from healthy donors


Elephant sample 6

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 6

text: Asiatic elephant

characteristic: common name

text: Elephant sample 1 to 8 used for RAD paired end sequencing

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample 3

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 3

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample A

text: SRA-Webin

text: IGC

text: public

text: Elephant sample A

text: Asiatic elephant

text: Genomic markers for Bornean elephant using 454 shotgun sequencing

text: Elephas maximus

text: Elephas maximus

text: Elephant samples A and B


Elephant sample 4

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 4

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample 2

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 2

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample 8

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 8

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample 1

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 1

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample 7

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 7

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample 5

text: SRA-Webin

text: IGC

text: public

text: Elephant sample 5

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Bornean elephant samples


Elephant sample B

text: SRA-Webin

text: IGC

text: public

text: Elephant sample B

text: Asiatic elephant

text: Elephas maximus

text: Elephas maximus

text: Elephant samples A and B


text: SRA-Webin

text: UMAC-ICMS

text: public

text: 1 of 10 samples, each sample consists of the NS segment from PR8 virus cloned into pMD 18-T vector and then mixed with mutant plasmids at different ratios for different samples

text: Influenza A virus (A/Puerto Rico/8/34/Mount Sinai(H1N1))

text: NS mix2


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix5


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix1


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix7


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix8


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix4


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix6


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix10


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix9


text: SRA-Webin

text: UMAC-ICMS

text: public

text: NS mix3


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy119 genome


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy34 genome


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy644 genome


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy209 genome


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy256 genome


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy717 genome


text: SRA-Webin

text: UP-IGM

text: public

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis

text: Percy556 genome


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Chromatin immunoprecipitation of Tcf7l2 transcription factor from Myc-335 null mouse colon tissue The sample was sequenced in two illumina lanes, this is the first lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon

characteristic: tissue type


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Negative IgG control for chromatin immunoprecipitation of Tcf7l2 transcription factor from wild type mouse colon tissue The sample was sequenced in two illumina lanes, this is the second lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Negative IgG control for chromatin immunoprecipitation of Tcf7l2 transcription factor from Myc-335 null mouse colon tissue. The sample was sequenced in two illumina lanes, this is the second lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Chromatin immunoprecipitation of Tcf7l2 transcription factor from Myc-335 null mouse colon tissue The sample was sequenced in two illumina lanes, this is the second lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Negative IgG control for chromatin immunoprecipitation of Tcf7l2 transcription factor from Myc-335 null mouse colon tissue. The sample was sequenced in two illumina lanes, this is the first lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Negative IgG control for chromatin immunoprecipitation of Tcf7l2 transcription factor from wild type mouse colon tissue The sample was sequenced in two illumina lanes, this is the first lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Chromatin immunoprecipitation of Tcf7l2 transcription factor from wild type mouse colon tissue. The sample was sequenced in two illumina lanes, this is the second lane of sequencing.

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: KI-BN

text: public

text: house mouse

text: Chromatin immunoprecipitation of Tcf7l2 transcription factor from wild type mouse colon tissue The sample was sequenced in two illumina lanes, this is the first lane of sequencing

text: Mus musculus

text: Mus musculus

text: colon


text: SRA-Webin

text: IM-CAU

text: public

characteristic: collection date

text: human gut microbiome

characteristic: environment (biome)

text: human gut

characteristic: environment (feature)

text: feces

characteristic: environment (material)

text: human-gut

characteristic: environmental package

text: South Korea

unit: DD

characteristic: geographic location (latitude)

characteristic: geographic location (longitude)

text: metagenome

characteristic: investigation type

text: human gut metagenome

text: Influence of Yogurt on Human Gut Microbiota

characteristic: project name

text: human gut metagenome

text: pyrosequencing

characteristic: sequencing method

text: during yogurt ingestion


characteristic: ENA-LAST-UPDATE

text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

characteristic: External Id

text: IM-CAU

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

characteristic: INSDC status

text: human gut microbiome

text: human gut

text: feces

text: human-gut

text: South Korea

text: metagenome

text: human gut metagenome

characteristic: organism

text: human gut metagenome

text: pyrosequencing

text: before yogurt ingestion

characteristic: title


characteristic: ENA-FIRST-PUBLIC

text: SRA-Webin

text: IM-CAU

text: public

characteristic: SRA accession

characteristic: Submitter Id

characteristic: collection date

text: human gut microbiome

characteristic: environment (biome)

text: human gut

characteristic: environment (feature)

text: feces

text: human-gut

text: South Korea

text: metagenome

text: human gut metagenome

text: human gut metagenome

text: pyrosequencing

text: after termination of yogurt ingestion


text: SRA-Webin

text: KTH

text: public

text: human

characteristic: common name

text: Homo sapiens

text: Homo sapiens


text: SRA-Webin

text: KTH

text: public

text: human

text: Homo sapiens

text: Homo sapiens


text: SRA-Webin

text: UNIVERISTY OF OXFORD

text: public

tag: Namespace:UNIVERISTY OF OXFORD

text: P000334 - TB sample from patient 334

characteristic: description

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis


characteristic: ENA-LAST-UPDATE

text: SRA-Webin

text: UNIVERISTY OF OXFORD

text: public

text: P000335 - TB sample from patient 335

text: Mycobacterium tuberculosis

text: Mycobacterium tuberculosis


text: BI-UK

text: public

text: house mouse

text: E16.5f RNA-Seq

text: Mus musculus

text: Mus musculus

text: female

characteristic: sex

characteristic: strain

characteristic: time

text: Primordial Germ Cell

characteristic: tissue


characteristic: External Id

text: BI-UK

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

text: house mouse

text: J1 BS-Seq 2

text: Mus musculus

text: Mus musculus

text: male

text: J1 ES Cell


characteristic: ENA-FIRST-PUBLIC

text: BI-UK

text: public

characteristic: INSDC status

text: house mouse

text: E6.5 BS-Seq 2

text: Mus musculus

characteristic: organism

text: Mus musculus

text: mixed

text: Epiblast


text: BI-UK

text: public

characteristic: SRA accession

characteristic: Submitter Id

text: house mouse

text: E13.5m RNA-Seq

text: Mus musculus

text: Mus musculus

text: male

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E9.5 BS-Seq 2

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E16.5f BS-Seq 1

text: Mus musculus

text: Mus musculus

text: female

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E6.5 BS-Seq 1

text: Mus musculus

text: Mus musculus

text: mixed

text: Epiblast


text: BI-UK

text: public

text: house mouse

text: E13.5f RNA-Seq

text: Mus musculus

text: Mus musculus

text: female

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E13.5f BS-Seq 1

text: Mus musculus

text: Mus musculus

text: female

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E11.5 BS-Seq 2

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E13.5m BS-Seq 2

text: Mus musculus

text: Mus musculus

text: male

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E16.5m BS-Seq 1

text: Mus musculus

text: Mus musculus

text: male

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E10.5 BS-Seq 1

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: J1 BS-Seq 1

text: Mus musculus

text: Mus musculus

text: male

text: J1 ES Cell


text: BI-UK

text: public

text: house mouse

text: E13.5m BS-Seq 1

text: Mus musculus

text: Mus musculus

text: male

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E11.5 RNA-Seq

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E10.5 BS-Seq 2

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E9.5 BS-Seq 1

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E13.5f BS-Seq 2

text: Mus musculus

text: Mus musculus

text: female

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E11.5 BS-Seq 1

text: Mus musculus

text: Mus musculus

text: mixed

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E16.5m RNA-Seq

text: Mus musculus

text: Mus musculus

text: male

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E16.5m BS-Seq 2

text: Mus musculus

text: Mus musculus

text: male

text: Primordial Germ Cell


text: BI-UK

text: public

text: house mouse

text: E16.5f BS-Seq 2

text: Mus musculus

text: Mus musculus

text: female

text: Primordial Germ Cell


status: KILLED

text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12885. We obtained the DNA sample NA12885 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12885 using the Illumina HiSeq 2000

characteristic: title


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

characteristic: common name

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12886. We obtained the DNA sample NA12886 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

characteristic: description

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12886 using the Illumina HiSeq 2000


characteristic: ENA-LAST-UPDATE

text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12887. We obtained the DNA sample NA12887 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12887 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12882 and is a technical replicate. We obtained the DNA sample NA12882 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12882 [technical replicate] using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12884. We obtained the DNA sample NA12884 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12884 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: public

characteristic: anonymized name

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12889. We obtained the DNA sample NA12889 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12889 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12888. We obtained the DNA sample NA12888 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12888 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12879. We obtained the DNA sample NA12879 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12879 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12893. We obtained the DNA sample NA12893 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12893 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: public

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12877. We obtained the DNA sample NA12877 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12877 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: public

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12891. We obtained the DNA sample NA12891 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12891 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: public

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12892. We obtained the DNA sample NA12892 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12892 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: public

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12890. We obtained the DNA sample NA12890 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12890 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: public

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12878. We obtained the DNA sample NA12878 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12878 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12881. We obtained the DNA sample NA12881 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12881 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12883. We obtained the DNA sample NA12883 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12883 using the Illumina HiSeq 2000


text: SRA-Webin

text: ILLUMINA

text: killed

text: human

text: We have generated paired-end sequence data covering the genome of an CEPH/UTAH individual to a sequence depth of more than 30-fold using the Illumina HiSeq 2000. This individual is a member of the CEPH/UTAH pedigree 1463 (abbreviation: CEPH). The DNA identifier for this individual is NA12882. We obtained the DNA sample NA12882 from The Coriell Institute for Medical Research. Starting with 1ug of DNA, and following random fragmentation, we generated a PCR-Free sequencing library with a median insert size of ~300 bp. 100 base sequence reads were generated from both ends of these templates using the Illumina HiSeq 2000. We carried out purity-filtering (PF) to remove mixed reads, where two or more different template molecules are close enough on the surface of the flow-cell to form a mixed or overlapping cluster. No other filtering of the data has been carried out prior to submission.

text: Homo sapiens

text: Homo sapiens

text: Whole genome sequencing of human individual NA12882 using the Illumina HiSeq 2000


text: SRA-Webin

text: DTU

text: public

text: Salmonella enterica subsp. enterica serovar Typhimurium


text: SRA-Webin

text: EBI

text: public

text: sample from Agilent OLS process, 153335 oligos each of length 183 nt including 33 nt paired-end adapter sequences at the 5ʹ and 3ʹ ends of each oligo

text: synthetic construct

text: synthetic construct

text: Agilent OLS

text: Emily LeProust, Agilent

text: Ewan Birney

text: synthetic DNA oligos designed for digital information storage


text: SRA-Webin

text: UU

text: public

text: DNA extracted from fossilised bone of Vindija Neandertal individual Vi33.16

text: fossil metagenome

text: fossil metagenome

text: fossil metagenome


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB15475


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma pos.EBV.EBV_1


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB17000


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB17809


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB18985


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB20080


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB16063


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb2.4.NB19388


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb2.4S.NB19696


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB15303


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB17861


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB19142


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB19388


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB18281


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4.NB17871


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB19696


text: SRA-Webin

text: MPI-INF

text: public

text: human

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma nb1.4S.NB15005


text: Shandong Agricultural University

text: public

text: inbred line Zheng 58

characteristic: StrainOrLine

text: ArrayExpress

characteristic: broker name

text: growth protocol: For collecting SL, seeds of Zheng 58 were surface-sterilized with 3 sodium hypochlorite for 10 min and rinsed in distilled water. Sterilized seeds were pre-germinated on moistened pledget in a plant growth chamber at 25C under 16/8 h light/dark cycle for about six days. Then we collected the whole seedling tissue as SL for RNA-seq analysis. For collecting the reproductive tissues including IMS, MS, MP, and MO, 20MAP and 3HAP plants were grown in silt loam soil at the Shandong Agricultural University experimental station in Tai an China (35 58N, 116 38E, 150m above sea level). Before tassels shedding pollens and silk growing from husk, we bagged the tassel and husk of experimental plants to prevent the pollination from pathogen and other plants. In the second to fifth days after anther dehiscence, mature pollen grains (MP) were collected in 1.5 mL Eppendorf tubes during 8:00-10:00am. After silks had grown from the husk for approximately three days, the upper parts (about 4 cm) of the silks were harvested as the mature silk tissues. After removing glumes around and silk on the top, whole mature ovaries distributed in a third part area in the middle of an ear were collected. The ear with the length of the longest silk length less than 1 cm was regarded as immature ear. Silks distributed in the center of the ear were collected as IMS materials. For collecting pollinated silks, each cob with mature silks was pollinated with about 0.3 g fresh mature pollen grains evenly, after shaking softly pollen grains which hadn't adhered to MS, the upper parts of silks (about 4 cm) at 20min and 3H after pollination were collected as the 20MAP and 3HAP materials. nucleic acid extraction protocol: Total RNA of each sample was extracted by using the hexadecyl trimethyl ammonium bromide (CTAB) protocol (Gambino et al., 2008)

text: pollination

characteristic: developmental stage

text: Zea mays

text: Zea mays

text: silk

characteristic: organism part

text: Zea mays


characteristic: External Id

text: Shandong Agricultural University

characteristic: INSDC center name

characteristic: INSDC first public

text: public

text: inbred line Zheng 58

text: ArrayExpress

text: Protocols: growth protocol: For collecting SL, seeds of Zheng 58 were surface-sterilized with 3G sodium hypochlorite for 10 min and rinsed in distilled water. Sterilized seeds were pre-germinated on moistened pledget in a plant growth chamber at 25C under 16/8 h light/dark cycle for about six days. Then we collected the whole seedling tissue as SL for RNA-seq analysis. For collecting the reproductive tissues including IMS, MS, MP, and MO, 20MAP and 3HAP plants were grown in silt loam soil at the Shandong Agricultural University experimental station in Tai an, China (35°58N, 116°38E, 150m above sea level). Before tassels shedding pollens and silk growing from husk, we bagged the tassel and husk of experimental plants to prevent the pollination from pathogen and other plants. In the second to fifth days after anther dehiscence, mature pollen grains (MP) were collected in 1.5 mL Eppendorf tubes during 8:00-10:00am. After silks had grown from the husk for approximately three days, the upper parts (about 4 cm) of the silks were harvested as the mature silk tissues. After removing glumes around and silk on the top, whole mature ovaries distributed in a third part area in the middle of an ear were collected. The ear with the length of the longest silk length less than 1 cm was regarded as immature ear. Silks distributed in the center of the ear were collected as IMS materials. For collecting pollinated silks, each cob with mature silks was pollinated with about 0.3 g fresh mature pollen grains evenly, after shaking softly pollen grains which hadn’t adhered to MS, the upper parts of silks (about 4 cm) at 20min and 3H after pollination were collected as the 20MAP and 3HAP materials. nucleic acid extraction protocol: Total RNA of MS was extracted by using TRIZOL reagent (Invitrogen, http://www.invitrogen.com) according to the manufacturers protocol, and the hexadecyl trimethyl ammonium bromide (CTAB) protocol was performed to extract the total RNA of MP, MO, and SL.

text: anthesis

text: Zea mays

text: Zea mays

text: silk

text: Zea mays

text: MS


characteristic: ENA-FIRST-PUBLIC

text: Shandong Agricultural University

characteristic: INSDC last update

text: public

characteristic: INSDC status

text: inbred line Zheng 58

text: ArrayExpress

text: Protocols: growth protocol: For collecting SL, seeds of Zheng 58 were surface-sterilized with 3G sodium hypochlorite for 10 min and rinsed in distilled water. Sterilized seeds were pre-germinated on moistened pledget in a plant growth chamber at 25C under 16/8 h light/dark cycle for about six days. Then we collected the whole seedling tissue as SL for RNA-seq analysis. For collecting the reproductive tissues including IMS, MS, MP, and MO, 20MAP and 3HAP plants were grown in silt loam soil at the Shandong Agricultural University experimental station in Tai an, China (35°58N, 116°38E, 150m above sea level). Before tassels shedding pollens and silk growing from husk, we bagged the tassel and husk of experimental plants to prevent the pollination from pathogen and other plants. In the second to fifth days after anther dehiscence, mature pollen grains (MP) were collected in 1.5 mL Eppendorf tubes during 8:00-10:00am. After silks had grown from the husk for approximately three days, the upper parts (about 4 cm) of the silks were harvested as the mature silk tissues. After removing glumes around and silk on the top, whole mature ovaries distributed in a third part area in the middle of an ear were collected. The ear with the length of the longest silk length less than 1 cm was regarded as immature ear. Silks distributed in the center of the ear were collected as IMS materials. For collecting pollinated silks, each cob with mature silks was pollinated with about 0.3 g fresh mature pollen grains evenly, after shaking softly pollen grains which hadn’t adhered to MS, the upper parts of silks (about 4 cm) at 20min and 3H after pollination were collected as the 20MAP and 3HAP materials.nucleic acid extraction protocol: Total RNA of MS was extracted by using TRIZOL reagent (Invitrogen, http://www.invitrogen.com) according to the manufacturers protocol, and the hexadecyl trimethyl ammonium bromide (CTAB) protocol was performed to extract the total RNA of MP, MO, and SL.

text: seedling

text: Zea mays

text: Zea mays

text: whole seedling

text: Zea mays

text: SL


text: Shandong Agricultural University

text: public

characteristic: SRA accession

text: inbred line Zheng 58

characteristic: Submitter Id

text: ArrayExpress

text: anthesis

text: Zea mays

characteristic: organism

text: Zea mays

text: ovary

text: Zea mays

text: MO


text: Shandong Agricultural University

text: public

text: inbred line Zheng 58

text: ArrayExpress

text: anthesis

text: Zea mays

text: Zea mays

text: pollen

text: Zea mays

text: MP

characteristic: title


text: Shandong Agricultural University

text: public

text: inbred line Zheng 58

text: ArrayExpress

characteristic: description

text: immature silk

text: Zea mays

text: Zea mays

text: silk

text: Zea mays

text: IMS


characteristic: ENA-LAST-UPDATE

text: public

tag: Namespace:Plate-forme Transcriptome et Epigenome, Institut Pasteur

characteristic: bio source type

text: CBS

characteristic: biosourceprovider

text: ArrayExpress

text: Protocols: batch culture in minimal media (yeast nitrogen base, YNB) containing different carbon sources at 28 degrees C Cell samples were harvested in the middle log phase, filtered at 0.22 um and flash frozen in liquid nitrogen Frozen cells have been disrupted using Sartorius mikrodismembrator (2 min at 2600 rpm). Total RNA were purified using Rneasy kit from Qiagen according to manufacturer's protocol.

text: mid log phase

text: wild type

characteristic: genotype

text: YNB with 2% glucose

characteristic: growth condition

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat A

characteristic: sex


characteristic: External Id

text: Plate-forme Transcriptome et Epigenome, Institut Pasteur

text: public

characteristic: StrainOrLine

text: CBS

text: ArrayExpress

characteristic: broker name

text: mid log phase

characteristic: developmental stage

text: wild type

text: YNB with 2% triolein

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat A


characteristic: ENA-FIRST-PUBLIC

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

text: CBS

text: ArrayExpress

text: mid log phase

text: wild type

text: YNB with 2% alkane (hexadecane)

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat A


text: public

characteristic: INSDC status

characteristic: SRA accession

characteristic: Submitter Id

text: CBS

text: ArrayExpress

text: mid log phase

text: wild type

text: YNB with 2% glycerol

text: Yarrowia lipolytica

characteristic: organism

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat A


characteristic: ENA-LAST-UPDATE

text: public

characteristic: bio source type

text: CBS

text: ArrayExpress

characteristic: description

text: mid log phase

text: wild type

text: YNB with 2% oleic Acid

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat A

characteristic: title


text: public

text: CBS

characteristic: biosourceprovider

text: ArrayExpress

text: mid log phase

text: wild type

characteristic: genotype

text: YNB with 2% tributyrin

characteristic: growth condition

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat A

characteristic: sex


characteristic: External Id

text: public

characteristic: StrainOrLine

text: INRA Micalis Institute / Biologie Intégrative du Métabolisme LIPidique microbien (BIMLip)

text: ArrayExpress

characteristic: broker name

text: Protocols: batch culture in Yeast Extract Peptone Dextrose (YPD) medium with 5% glucose at 28 degrees C Cell samples were harvested in the middle log phase and flash frozen in liquid nitrogen Frozen cells have been disrupted using Sartorius mikrodismembrator (2 min at 2600 rpm). Total RNA were purified using Rneasy kit from Qiagen according to manufacturer's protocol.

text: mid log phase

characteristic: developmental stage

text: his-1, ura3-302, xpr2-322, delta-Ku70::ura3

text: YPD 2%

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Yarrowia lipolytica

text: Mat B


characteristic: ENA-FIRST-PUBLIC

text: SRA-Webin

characteristic: ENA-SUBMISSION-TOOL

text: CRG

characteristic: INSDC center name

characteristic: INSDC first public

characteristic: INSDC last update

text: public

text: pcan brain Queen175

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Queen175


characteristic: ENA-LAST-UPDATE

text: SRA-Webin

text: CRG

text: public

characteristic: INSDC status

characteristic: SRA accession

characteristic: Submitter Id

text: Polistes canadensis

characteristic: organism

text: Polistes canadensis

text: pcan brain Foundress Co-Dominant


text: SRA-Webin

text: CRG

text: public

characteristic: description

text: Polistes canadensis

text: Polistes canadensis

characteristic: title


text: SRA-Webin

text: CRG

text: public

text: pcan brain Worker156

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Worker156


text: SRA-Webin

text: CRG

text: public

text: pcan brain Foundress Dominant

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Foundress Dominant


text: SRA-Webin

text: CRG

text: public

text: pcan brain Worker108

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Worker108


text: SRA-Webin

text: CRG

text: public

text: pcan brain Queen178

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Queen178


text: SRA-Webin

text: CRG

text: public

text: pcan brain Newly Emerged08

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Newly Emerged08


text: SRA-Webin

text: CRG

text: public

text: pcan brain Newly Emerged09

text: Polistes canadensis

text: Polistes canadensis

text: pcan brain Newly Emerged09


LL-Ga

text: SRA-Webin

text: CURIE

text: public

text: LL-Ga

text: LL-Ga

characteristic: anonymized name

text: human

characteristic: common name

text: Lymphoblastoid cell line LL-Ga matching the CLB-Ga neuroblastoma cell line

text: Homo sapiens

text: Homo sapiens

text: Lymphoblastoid cell line LL-Ga


CLB-Ga

text: SRA-Webin

characteristic: External Id

text: CURIE

text: public

text: CLB-Ga

text: CLB-Ga

text: human

text: Neuroblastoma cell line CLB-Ga

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma cell line CLB-Ga


CLB-Re

text: SRA-Webin

text: CURIE

text: public

text: CLB-Re

text: CLB-Re

text: human

text: Neuroblastoma cell line CLB-Re

text: Homo sapiens

text: Homo sapiens

text: Neuroblastoma cell line CLB-Re


text: SRA-Webin

text: CURIE

text: public

text: human

text: neuroblastoma primary tumor NB1142 exhibiting chromothripsis

text: Homo sapiens

text: Homo sapiens

text: neuroblastoma primary tumor NB1142