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SRX194836: Low Coverage Genome Sequencing
8 ILLUMINA (Illumina HiSeq 2000) runs: 17.5M spots, 3.5G bases, 1.7Gb downloads

UUID: 52c916bf-83b4-47d0-8bc9-ba252d0a8403
Design: Low Coverage Genome Sequencing
Submitted by: Broad Institute (BI)
Study: Whole genome sequencing of (PJL) Punjabi HapMap population
Sample: Coriell HG02600
SAMN00779993 • SRS290930 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Sage-109752
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:3DAZY
project: G22850
sample_barcode: 219804.0
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, 17.5M spots, 3.5G bases, 1.7Gb
Run# of Spots# of BasesSizePublished
SRR5888432,180,209440.4M211.2Mb2012-10-13
SRR5889022,183,057441M212.4Mb2012-10-13
SRR5890142,153,280435M206.6Mb2012-10-13
SRR5890262,169,425438.2M211.3Mb2012-10-13
SRR5896102,179,845440.3M210Mb2012-10-13
SRR5898602,180,616440.5M213.6Mb2012-10-13
SRR5901002,146,166433.5M210.7Mb2012-10-13
SRR5901192,261,235456.8M221.7Mb2012-10-13

ID:
257840

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