Illumina NovaSeq 6000 paired end sequencing - SRA

ERX8898684: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 28.1M spots, 8.5G bases, 2.6Gb downloads

Design: Illumina sequencing of sample accession SAMEA12928264 for study accession PRJEB51747. This is part of an Illumina multiplexed sequencing run (35778_1). This submission includes reads tagged with the sequence CCTACGTA.

Submitted by: Wellcome Sanger Institute

Study: Anopheles cruzii, genomic and transcriptomic data

PRJEB51747 • ERP136399 • All experiments • All runs

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This project collects the genomic and transcriptomic data generated for the mosquito species Anopheles cruzii to facilitate genome assembly and annotation as part of the Anopheles Reference Genomes project. These data (including raw data and assemblies) are released for reuse for any purpose upon deposition in ENA, and we encourage reuse. More information on Sanger's data release policy can be found here https://www.sanger.ac.uk/about/who-we-are/research-policies/open-access-science/.

Sample: 19390-tol

SAMEA12928264 • ERS10527397 • All experiments • All runs

Organism: Anopheles cruzii

Library:

Instrument: Illumina NovaSeq 6000

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Chromium genome

Runs: 1 run, 28.1M spots, 8.5G bases, 2.6Gb

Run	# of Spots	# of Bases	Size	Published
ERR9356782	28,116,727	8.5G	2.6Gb	2022-03-25

ID:: 20856530

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