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SRX9352297: Genome sequencing of C. neoformans var grubii
1 ILLUMINA (Illumina HiSeq 2500) run: 7.9M spots, 2.4G bases, 1,000.8Mb downloads

Design: DNA libraries were sequenced using Illumina HiSeq with 150 base pair paired end reads
Submitted by: Pontificia Universidad Javeriana
Study: Cryptococcus neoformans var. grubii Genome sequencing
show Abstracthide Abstract
Genome sequencing of 29 clinical isolates of Cryptococcus neoformans var. grubii
Sample: Cneo_3104
SAMN16533797 • SRS7575607 • All experiments • All runs
Library:
Name: Cneo_3104
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Runs: 1 run, 7.9M spots, 2.4G bases, 1,000.8Mb
Run# of Spots# of BasesSizePublished
SRR128866307,875,2422.4G1,000.8Mb2021-06-01

ID:
12213217

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