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ERX215046: Whole Genome Sequencing of human CHB NA18626
1 ILLUMINA (Illumina HiSeq 2000) run: 2.1M spots, 420M bases, 202Mb downloads

Design: Illumina sequencing of library 6504035, constructed from sample accession SRS000680 for study accession SRP000546. This is part of an Illumina multiplexed sequencing run (9378_5). This submission includes reads tagged with the sequence TTGACTCT.
Submitted by: The Wellcome Trust Sanger Institute (SC)
Study: Whole genome sequencing of (CHB) Han Chinese in Beijing, China HapMap population
PRJNA33851 • SRP000546 • All experiments • All runs
Sample: Coriell GM18626
SAMN00000450 • SRS000680 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 6504035
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 2.1M spots, 420M bases, 202Mb
Run# of Spots# of BasesSizePublished
ERR2405122,100,127420M202Mb2013-03-22

ID:
344420

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