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ERX12671813: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 187.1M spots, 53.9G bases, 16.5Gb downloads

Design: Illumina sequencing of library SQPP-6558-A:H6, constructed from sample accession ERS14853718 for study accession ERP145941. This is part of an Illumina multiplexed sequencing run (47486). This submission includes reads tagged with the sequence CAAATAGC.
Submitted by: Wellcome Sanger Institute
Study: Cross_Species_Bulk_Blood_whole_genome_nanoseq
show Abstracthide Abstract
The somatic mutational landscape of different species will be characterized using nanoseq. Samples have been sourced from the Cambridge Biobank
Sample: WRHD0002c_ds0001
SAMEA112847113 • ERS14853718 • All experiments • All runs
Library:
Name: SQPP-6558-A:H6
Instrument: Illumina NovaSeq 6000
Strategy: AMPLICON
Source: GENOMIC
Selection: PCR
Layout: PAIRED
Construction protocol: Duplex-Seq
Runs: 1 run, 187.1M spots, 53.9G bases, 16.5Gb
Run# of Spots# of BasesSizePublished
ERR13300951187,121,78753.9G16.5Gb2024-07-28

ID:
34351806

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