SRA

ERX006476: Whole Genome Sequencing of human FIN
1 ILLUMINA (Illumina Genome Analyzer II) run: 34.8M spots, 3.1G bases, 1.3Gb downloads

Design: Solexa sequencing of Human individual HG00315 random pair end library

Submitted by: Beijing Genome Institute (BGI)

Study: Whole genome sequencing of (FIN) Finnish in Finland HapMap population

Sample: Coriell HG00315

Library:

Name: HUMgfvRBEDIAAPE

Instrument: Illumina Genome Analyzer II

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Standard Solexa protocol

Spot descriptor:

1 forward46 reverse

Experiment attributes:

center_name: BGI

Runs: 1 run, 34.8M spots, 3.1G bases, 1.3Gb

Run	# of Spots	# of Bases	Size	Published
ERR016239	34,830,036	3.1G	1.3Gb	2010-09-14

Supplemental Content

32139[uid] (1)
SRA
Ocular albinism
Ocular albinism

MedGen
C0078917[conceptid] (1)
MedGen
Refractory B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1
Refractory B Acute Lymphoblastic Leukemia with t(9;22)(q34.1;q11.2); BCR-ABL1

MedGen
PCGF1 polycomb group ring finger 1 [Gallus gallus]
PCGF1 polycomb group ring finger 1 [Gallus gallus]
Gene ID:100858619

Gene

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Sequence Read Archive