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ERX225603: Whole Genome Sequencing of human FIN
1 ILLUMINA (Illumina HiSeq 2000) run: 49M spots, 9.8G bases, 6.2Gb downloads

Design: Solexa sequencing of Human individual HG00383 random pair end library
Submitted by: Beijing Genome Institute (BGI)
Study: Whole genome sequencing of (FIN) Finnish in Finland HapMap population
Sample: Coriell HG00383
SAMN00009113 • SRS010744 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: SZAIPI021780-136
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard Solexa protocol
Spot descriptor:
forward101  reverse

Experiment attributes:
center_name: BGI
Runs: 1 run, 49M spots, 9.8G bases, 6.2Gb
Run# of Spots# of BasesSizePublished
ERR25106948,992,6669.8G6.2Gb2013-04-16

ID:
363933

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