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ERX225642: Whole Genome Sequencing of human CHS
1 ILLUMINA (Illumina HiSeq 2000) run: 58.5M spots, 11.7G bases, 8.1Gb downloads

Design: Solexa sequencing of Human individual HG00478 random pair end library
Submitted by: Beijing Genome Institute (BGI)
Study: Whole genome sequencing of (CHS) Southern Han Chinese population HapMap population
PRJNA41139 • SRP001293 • 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. DNA for this sample was extracted from lymphoblastoid cell line.
Sample: Coriell HG00478
SAMN00006459 • SRS008625 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: SZAIPI022190-27
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard Solexa protocol
Spot descriptor:
1  forward101  reverse

Experiment attributes:
center_name: BGI
Runs: 1 run, 58.5M spots, 11.7G bases, 8.1Gb
Run# of Spots# of BasesSizePublished
ERR25110858,486,57511.7G8.1Gb2013-04-16

ID:
363970

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