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SRX042613: Whole Exome sequencing for the 1000 Genomes Project
7 ILLUMINA (Illumina HiSeq 2000) runs: 16.2M spots, 2.6G bases, 1.5Gb downloads

Design: Whole Exome sequencing for the 1000 Genomes Project via in-solution hybrid selection
Submitted by: Broad Institute (BI)
Study: Exome sequencing of (CHS) Southern Han Chinese population HapMap population
PRJNA60155 • SRP004365 • All experiments • All runs
Sample: Coriell HG00611
SAMN00006517 • SRS008683 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: Catch-49027
Instrument: Illumina HiSeq 2000
Strategy: WXS
Source: GENOMIC
Selection: Hybrid Selection
Layout: PAIRED
Spot descriptor:
1  forward barcode85  reverse

Experiment attributes: (show all 5 attributes...) (hide...)
EXPECTED_BASECALL_TABLE: match_edge="full" max_mismatch="1" min_match="7" r (show full text...)(hide...)
match_edge="full" max_mismatch="1" min_match="7" read_group_tag="tagged_289" member_name="tagged_289_ATTATGTT" ATTATGTT
4 BI attributes: (show...)(hide...)
BI GSSR sample ID: 80959.0
BI GSSR sample LSID: broadinstitute.org:bsp.prod.sample:1NNFW
BI project name: C459
BI work request ID: 24132
Runs: 7 runs, 16.2M spots, 2.6G bases, 1.5Gb
Run# of Spots# of BasesSizePublished
SRR1003342,296,660367.5M220.9Mb2011-02-15
SRR1003372,389,076382.3M230.1Mb2011-02-15
SRR1003672,295,509367.3M219.5Mb2011-02-15
SRR1003752,349,977376M226.6Mb2011-02-15
SRR1003922,321,458371.4M223.2Mb2011-02-15
SRR1003952,354,896376.8M226.1Mb2011-02-15
SRR1004332,224,332355.9M214Mb2011-02-15

ID:
50885

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