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SRX194921: Low Coverage Genome Sequencing
8 ILLUMINA (Illumina HiSeq 2000) runs: 19.3M spots, 3.9G bases, 1.8Gb downloads

UUID: 3d444e50-707b-48d5-a0a6-4c5091523940
Design: Low Coverage Genome Sequencing
Submitted by: Broad Institute (BI)
Study: Whole genome sequencing of (PJL) Punjabi HapMap population
PRJNA59833 • SRP004077 • All experiments • All runs
Sample: Coriell HG02601
SAMN00779994 • SRS290931 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Sage-109751
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:3DAZX
project: G22849
sample_barcode: 219803.0
work_request: 31670
Pipeline: show...hide...
NameStepProgramVersionNotes
base caller2012-08-27 22:01:52.0GAPipelineRTA1.13.48Sequencer Application 1.5.15.1
Runs: 8 runs, 19.3M spots, 3.9G bases, 1.8Gb
Run# of Spots# of BasesSizePublished
SRR5898072,407,244486.3M232.3Mb2012-10-13
SRR5898732,502,686505.5M244.4Mb2012-10-13
SRR5900282,406,123486M230.9Mb2012-10-13
SRR5901072,393,747483.5M232.2Mb2012-10-13
SRR5901582,364,411477.6M230.9Mb2012-10-14
SRR5902572,407,401486.3M233.3Mb2012-10-14
SRR5904582,369,916478.7M226.2Mb2012-10-14
SRR5906292,411,974487.2M235.1Mb2012-10-14

ID:
257932

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