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ERX10912433: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 1.5M spots, 445.9M bases, 58.1Mb downloads

Design: Illumina sequencing of library DN924901V:N12, constructed from sample accession ERS11967128 for study accession ERP001039. This is part of an Illumina multiplexed sequencing run (44994_1). This submission includes reads tagged with the sequence GGCCGTTG.
Submitted by: Wellcome Sanger Institute
Study: Whole_genome_sequencing_of_pathogenic_strains_of_Mycobacterium_abscessus
show Abstracthide Abstract
http://www.sanger.ac.uk/resources/downloads/bacteria/mycobacterium.html
Sample: T0_5_b
SAMEA14372609 • ERS11967128 • All experiments • All runs
Library:
Name: DN924901V:N12
Instrument: Illumina NovaSeq 6000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: pWGS-384
Runs: 1 run, 1.5M spots, 445.9M bases, 58.1Mb
Run# of Spots# of BasesSizePublished
ERR115065531,476,576445.9M58.1Mb2023-09-16

ID:
29567818

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