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ERX215035: Whole Genome Sequencing of human CHB NA18627
1 ILLUMINA (Illumina HiSeq 2000) run: 1.9M spots, 388M bases, 189.4Mb downloads

Design: Illumina sequencing of library 6503952, constructed from sample accession SRS000681 for study accession SRP000546. This is part of an Illumina multiplexed sequencing run (9378_2). This submission includes reads tagged with the sequence TGCGATCT.
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 GM18627
SAMN00000451 • SRS000681 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: 6503952
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 1.9M spots, 388M bases, 189.4Mb
Run# of Spots# of BasesSizePublished
ERR2405011,939,878388M189.4Mb2013-03-22

ID:
344409

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