Illumina HiSeq 2500 paired end sequencing - SRA

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ERX2666555: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 1.5M spots, 364.6M bases, 119.6Mb downloads

Design: Illumina sequencing of library DN445031H:B7, constructed from sample accession ERS1106271 for study accession ERP014540. This is part of an Illumina multiplexed sequencing run (19944_6). This submission includes reads tagged with the sequence TATGTGGC.

Submitted by: SC (The Wellcome Trust Sanger Institute)

Study: GAS_Vaccinology__Capturing_Global_Vaccine_Antigen_Diversity

PRJEB13003 • ERP014540 • All experiments • All runs

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This project consists of a two-phase action plan designed to validate the overall aims of the GAS vaccinology programme as well as generating publishable units from scientifically robust comparisons. Apart from vaccine antigen design, this programme of sequencing will support targeted analyses of specific disease associations and global transmission patterns of prominent sequence types- all ongoing sequencing based research foci that Sanger (Mark Davies) is currently analysing.

Sample: 19944_6#137

SAMEA3919137 • ERS1106271 • All experiments • All runs

Organism: Streptococcus pyogenes

Library:

Name: DN445031H:B7

Instrument: Illumina HiSeq 2500

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Standard

Runs: 1 run, 1.5M spots, 364.6M bases, 119.6Mb

Run	# of Spots	# of Bases	Size	Published
ERR2650065	1,458,447	364.6M	119.6Mb	2018-07-04

ID:: 5872877

SRA

Sequence Read Archive

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