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SRX195215: Low Coverage Genome Sequencing
1 ILLUMINA (Illumina HiSeq 2000) run: 2.3M spots, 457.2M bases, 236Mb downloads

UUID: b33e3c99-2637-46de-bca8-b77b0850339d
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 HG00599
SAMN01036843 • SRS344111 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Sage-109737
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:3DAZJ
project: G22826
sample_barcode: 219789.0
work_request: 31670
Pipeline: show...hide...
NameStepProgramVersionNotes
base caller2012-08-27 21:21:23.0GAPipelineRTA1.13.48Sequencer Application 1.5.15.1
Runs: 1 run, 2.3M spots, 457.2M bases, 236Mb
Run# of Spots# of BasesSizePublished
SRR5921092,263,238457.2M236Mb2012-10-14

ID:
258226

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