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ERX006368: Whole Genome Sequencing of human CHS
1 ILLUMINA (Illumina Genome Analyzer IIx) run: 32.3M spots, 4.8G bases, 2Gb downloads

Design: Solexa sequencing of Human individual HG00531 random pair end library.Since one lane equated to one sample and for technical reasons, the barcode was removed prior to submission. This makes the read pairs uneven in length.
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 HG00531
SAMN00006472 • SRS008638 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: HUMgqcREIDIAAPEI-7
Instrument: Illumina Genome Analyzer IIx
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard Solexa protocol
Spot descriptor:
1  forward82  reverse

Experiment attributes:
center_name: BGI
Runs: 1 run, 32.3M spots, 4.8G bases, 2Gb
Run# of Spots# of BasesSizePublished
ERR01613132,258,4474.8G2Gb2010-09-14

ID:
32211

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