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SRX195245: Low Coverage Genome Sequencing
8 ILLUMINA (Illumina HiSeq 2000) runs: 16.7M spots, 3.4G bases, 1.5Gb downloads

UUID: 7eb3ed9f-cb67-4b03-afaf-25d886271b6d
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 HG00675
SAMN01036855 • SRS344123 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Sage-109733
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:3DAZF
project: G22825
sample_barcode: 219785.0
work_request: 31670
Pipeline: show...hide...
NameStepProgramVersionNotes
base caller2012-08-27 21:46:41.0GAPipelineRTA1.13.48Sequencer Application 1.5.15.1
Runs: 8 runs, 16.7M spots, 3.4G bases, 1.5Gb
Run# of Spots# of BasesSizePublished
SRR5922412,084,687421.1M197.5Mb2012-10-15
SRR5933372,074,037419M195.6Mb2012-10-16
SRR5933552,084,088421M198.5Mb2012-10-16
SRR5934662,060,514416.2M194.7Mb2012-10-16
SRR5934692,114,907427.2M203Mb2012-10-16
SRR5935312,104,635425.1M197.6Mb2012-10-16
SRR5935502,088,378421.9M196.3Mb2012-10-16
SRR5936512,079,856420.1M197.3Mb2012-10-16

ID:
258256

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