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ERX006998: Whole Genome Sequencing of human FIN
1 ILLUMINA (Illumina Genome Analyzer II) run: 42.3M spots, 6.4G bases, 2.8Gb downloads

Design: Solexa sequencing of Human individual HG00330 random pair end library
Submitted by: Beijing Genome Institute (BGI)
Study: Whole genome sequencing of (FIN) Finnish in Finland HapMap population
Sample: Coriell HG00330
SAMN00009108 • SRS010739 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: HUMgxiRCVDIAAPE
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard Solexa protocol
Spot descriptor:
forward77  reverse

Experiment attributes:
center_name: BGI
Runs: 1 run, 42.3M spots, 6.4G bases, 2.8Gb
Run# of Spots# of BasesSizePublished
ERR01846942,275,3616.4G2.8Gb2010-12-16

ID:
36454

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