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ERX007029: Whole Genome Sequencing of human FIN
1 ILLUMINA (Illumina Genome Analyzer II) run: 15.1M spots, 3.3G bases, 1.9Gb downloads

Design: Illumina sequencing of Homo sapiens g1k-sc-HG00182-A library
Submitted by: The Wellcome Trust Sanger Institute (SC)
Study: Whole genome sequencing of (FIN) Finnish in Finland HapMap population
PRJNA38449 • SRP000808 • All experiments • All runs
Sample: Coriell HG00182
SAMN00016974 • SRS006901 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: g1k-sc-HG00182-A
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Spot descriptor:
1  forward109  reverse

Runs: 1 run, 15.1M spots, 3.3G bases, 1.9Gb
Run# of Spots# of BasesSizePublished
ERR01850715,053,9763.3G1.9Gb2010-12-16

ID:
36485

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