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SRX25673041: Whole-genome sequencing of Cryptococcus neformans: mutants
1 ILLUMINA (Illumina NovaSeq X Plus) run: 81.1M spots, 24.5G bases, 6.9Gb downloads

Design: Genomic DNA was prepared and subjected to Illumina sequencing. The library preparation and sequencing was performed as per the manufacturer's instructions
Submitted by: Duke University Medical Center
Study: Cryptococcus neoformans var. grubii Raw sequence reads
show Abstracthide Abstract
Sequence reads from Illumina whole-genome sequencing of Cryptococcus neoformans isolates from H99 and KN99 haploid, and KN99a/KN99alpha diploid backgrounds. Used to confirm deletion mutations generated in the indicated strain backgrounds, and analyze read depth to find regions of aneuploidy in these isolates.
Sample:
SAMN43092201 • SRS22314961 • All experiments • All runs
Library:
Name: YSB9100
Instrument: Illumina NovaSeq X Plus
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Runs: 1 run, 81.1M spots, 24.5G bases, 6.9Gb
Run# of Spots# of BasesSizePublished
SRR3021001581,132,67324.5G6.9Gb2024-08-12

ID:
34693978

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