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SRX9805595: Blood Whole Exome Sequencing of Congenital stationary night blindness, CSNB - Patient 1
1 ILLUMINA (NextSeq 500) run: 24.8M spots, 7.4G bases, 3.3Gb downloads

Design: Libraries were generated using the Topomize DNA LT Library Prep Kit and the hybridization capture of DNA libraries was performed with xGen Lockdown panels to generate 150-bp paired-end reads
Submitted by: Seoul National University Hospital
Study: Whole-Exome Sequencing in Korean Patients with Inherited Retinal Degeneration
PRJNA690657 • SRP300863 • All experiments • All runs
Sample: Blood - Congenital stationary night blindness, CSNB - Patient 1
SAMN17256362 • SRS7989670 • All experiments • All runs
Organism: Homo sapiens
Library:
Name: CASEID_104_WES
Instrument: NextSeq 500
Strategy: WXS
Source: GENOMIC
Selection: Hybrid Selection
Layout: PAIRED
Runs: 1 run, 24.8M spots, 7.4G bases, 3.3Gb
Run# of Spots# of BasesSizePublished
SRR1338624924,758,2957.4G3.3Gb2021-01-08

ID:
12839634

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