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ERX225599: Whole Genome Sequencing of human FIN
1 ILLUMINA (Illumina HiSeq 2000) run: 71.6M spots, 14.3G bases, 10.2Gb downloads

Design: Solexa sequencing of Human individual HG00378 random pair end library
Submitted by: Beijing Genome Institute (BGI)
Study: Whole genome sequencing of (FIN) Finnish in Finland HapMap population
PRJNA38449 • SRP000808 • All experiments • All runs
Sample: Coriell HG00378
SAMN00006426 • SRS008592 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: SZAIPI021777-123
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard Solexa protocol
Spot descriptor:
1  forward101  reverse

Experiment attributes:
center_name: BGI
Runs: 1 run, 71.6M spots, 14.3G bases, 10.2Gb
Run# of Spots# of BasesSizePublished
ERR25106571,631,17014.3G10.2Gb2013-04-16

ID:
363929

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