Blood Whole Exome Sequencing of Congenital stationary night blindness... - SRA

SRX9805488: Blood Whole Exome Sequencing of Congenital stationary night blindness, CSNB - Patient 2
1 ILLUMINA (NextSeq 500) run: 18M spots, 5.4G bases, 2.4Gb 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 2

SAMN17256418 • SRS7989563 • All experiments • All runs

Organism: Homo sapiens

Library:

Name: CASEID_164_WES

Instrument: NextSeq 500

Strategy: WXS

Source: GENOMIC

Selection: Hybrid Selection

Layout: PAIRED

Runs: 1 run, 18M spots, 5.4G bases, 2.4Gb

Run	# of Spots	# of Bases	Size	Published
SRR13386356	18,005,486	5.4G	2.4Gb	2021-01-08

ID:: 12839527

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