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SRX194721: Low Coverage Genome Sequencing
8 ILLUMINA (Illumina HiSeq 2000) runs: 21.8M spots, 4.4G bases, 2.1Gb downloads

UUID: 52a0e860-8966-4898-b65f-9773917ef493
Design: Low Coverage Genome Sequencing
Submitted by: Broad Institute (BI)
Study: Whole genome sequencing of (PJL) Punjabi HapMap population
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:
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 caller2012-08-24 02:03:26.0GAPipelineRTA1.13.48Sequencer Application 1.5.15.1
Runs: 8 runs, 21.8M spots, 4.4G bases, 2.1Gb
Run# of Spots# of BasesSizePublished
SRR5886062,719,505549.3M269.5Mb2012-10-13
SRR5886472,774,944560.5M278.6Mb2012-10-13
SRR5898332,719,721549.4M271.7Mb2012-10-13
SRR5899502,730,286551.5M272.9Mb2012-10-13
SRR5900712,707,233546.9M268.2Mb2012-10-13
SRR5902792,763,865558.3M278.1Mb2012-10-14
SRR5903652,722,567550M270.9Mb2012-10-14
SRR5904762,639,397533.2M265.1Mb2012-10-14

ID:
257725

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