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SRX195231: Low Coverage Genome Sequencing
8 ILLUMINA (Illumina HiSeq 2000) runs: 18.7M spots, 3.8G bases, 1.8Gb downloads

UUID: 624f9dd8-ad82-4f16-9015-c29c44e8f079
Design: Low Coverage Genome Sequencing
Submitted by: Broad Institute (BI)
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 HG00623
SAMN01036849 • SRS344117 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Sage-109742
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Spot descriptor:
1  forward102  reverse

Experiment attributes: (show all 4 attributes...) (hide...)
lsid: broadinstitute.org:bsp.prod.sample:3DAZO
project: G22830
sample_barcode: 219794.0
work_request: 31670
Pipeline: show...hide...
NameStepProgramVersionNotes
base caller2012-08-27 22:05:34.0GAPipelineRTA1.13.48Sequencer Application 1.5.15.1
Runs: 8 runs, 18.7M spots, 3.8G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR5921472,295,259463.6M229.5Mb2012-10-15
SRR5933702,366,266478M240.6Mb2012-10-16
SRR5937542,333,360471.3M232.7Mb2012-10-17
SRR5939132,312,288467.1M231.9Mb2012-10-17
SRR5939622,354,367475.6M236.9Mb2012-10-17
SRR5939892,314,102467.4M232.4Mb2012-10-17
SRR5940042,366,676478.1M241.3Mb2012-10-17
SRR5940422,372,020479.1M238.8Mb2012-10-17

ID:
258242

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