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ERX1124863: Illumina HiSeq 2000 paired end sequencing; NA18594_HUMiqvDBLDBADPE_FC80EH2ABXX_L5
1 ILLUMINA (Illumina HiSeq 2000) run: 89.2M spots, 17.8G bases, 9.9Gb downloads

Design: The purpose of the project is to support the discovery and understanding of genetic variants that influence human disease, with particular emphasis on the Chinese population.
Submitted by: Beijing Genome Institute (BGI)
Study: High-coverage whole genome sequencing of Han Chinese populations (1000 Genomes Project)
PRJEB11005 • ERP012319 • All experiments • All runs
show Abstracthide Abstract
The purpose of the project is to support the discovery and understanding of genetic variants that influence human disease, with particular emphasis on the Chinese population. Here we provide whole genome sequence data on 91 individuals of Chinese origin.
Sample: HapMap sample from Homo sapiens
SAMN00007636 • SRS003570 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: HUMiqvDBLDBADPE
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Runs: 1 run, 89.2M spots, 17.8G bases, 9.9Gb
Run# of Spots# of BasesSizePublished
ERR104457289,158,46117.8G9.9Gb2015-10-27

ID:
1884687

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