Illumina HiSeq 2500 paired end sequencing - SRA - NCBI

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ERX3961658: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 548,348 spots, 274.2M bases, 138.2Mb downloads

Design: Illumina sequencing of library DN443491A:E6, constructed from sample accession ERS4332897 for study accession ERP005466. This is part of an Illumina multiplexed sequencing run (19961_2). This submission includes reads tagged with the sequence TATGCCAG.

Submitted by: Wellcome Sanger Institute

Study: ICONIC

PRJEB6008 • ERP005466 • All experiments • All runs

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Sample: 3034STDY6355675

SAMEA6568562 • ERS4332897 • All experiments • All runs

Organism: HIV-1 unknown group

Library:

Name: DN443491A:E6

Instrument: Illumina HiSeq 2500

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Standard

Runs: 1 run, 548,348 spots, 274.2M bases, 138.2Mb

Run	# of Spots	# of Bases	Size	Published
ERR3953853	548,348	274.2M	138.2Mb	2020-02-28

ID:: 10226399

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ERR3953853 (1)
SRA
BRCA1 BRCA1 DNA repair associated [Homo sapiens]
BRCA1 BRCA1 DNA repair associated [Homo sapiens]
Gene ID:672

Gene
Gene Links for Nucleotide (Select 2249007046) (1)
Gene
Homo sapiens BRCA1 DNA repair associated (BRCA1), transcript variant 52, mRNA
Homo sapiens BRCA1 DNA repair associated (BRCA1), transcript variant 52, mRNA
gi|2249007046|ref|NM_001407640.1|

Nucleotide

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