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ERX2274651: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 2M spots, 506.2M bases, 165Mb downloads

Design: Illumina sequencing of library DN446969G:D12, constructed from sample accession ERS2046386 for study accession ERP105624. This is part of an Illumina multiplexed sequencing run (20287_6). This submission includes reads tagged with the sequence GCCTGTTC.
Submitted by: Wellcome Sanger Institute
Study: Genomic_and_bacterial_blueprint_of_the_human_gastrointestinal_microbiota
show Abstracthide Abstract
Here we present a comprehensive collection of 737 whole-genome sequenced bacterial isolates from humans to understand the blueprint of human gastrointestinal microbiota.
Sample: V4.EO
SAMEA104428444 • ERS2046386 • All experiments • All runs
Library:
Name: DN446969G:D12
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 2M spots, 506.2M bases, 165Mb
Run# of Spots# of BasesSizePublished
ERR22212782,024,618506.2M165Mb2019-01-24

ID:
7124519

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