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SRX195247: Low Coverage Genome Sequencing
8 ILLUMINA (Illumina HiSeq 2000) runs: 18.5M spots, 3.7G bases, 1.8Gb downloads

UUID: 04b0362f-741a-4c68-8a0c-c4b1ddae1fe4
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 HG00409
SAMN01036839 • SRS344107 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Sage-109727
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:3DAZ9
project: G22823
sample_barcode: 219780.0
work_request: 31670
Pipeline: show...hide...
NameStepProgramVersionNotes
base caller2012-08-24 02:03:26.0GAPipelineRTA1.13.48Sequencer Application 1.5.15.1
Runs: 8 runs, 18.5M spots, 3.7G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR5921732,314,236467.5M232.8Mb2012-10-15
SRR5934712,312,986467.2M231.4Mb2012-10-16
SRR5936682,312,881467.2M230.5Mb2012-10-16
SRR5937252,245,697453.6M226.7Mb2012-10-17
SRR5938392,353,852475.5M237.9Mb2012-10-17
SRR5939512,301,154464.8M229.3Mb2012-10-17
SRR5940642,348,946474.5M238Mb2012-10-17
SRR5941072,306,375465.9M231.6Mb2012-10-17

ID:
258258

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