Illumina NovaSeq 6000 paired end sequencing - SRA

ERX3898875: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 721.3M spots, 217.8G bases, 64Gb downloads

Submitted by: UNIVERSITY OF CALIFORNIA - DAVIS

Study: Whole Genome Sequencing Identifies Missense Mutation in GRM6 as the Likely Cause of Congenital Stationary Night Blindness in a Tennessee Walking Horse

PRJEB36381 • ERP119570 • All experiments • All runs

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To identify sequencing variant(s) causal for Congenital Stationary Night Blindness in a Tennessee Walking Horse, we performed whole genome sequencing of at least 20X coverage on the Nova-Seq platform.

Sample: Whole Genome Sequencing Identifies Missense Mutation in GRM6 as the Likely Cause of Congenital Stationary Night Blindness in a Tennessee Walking Horse

SAMEA6527628 • ERS4292032 • All experiments • All runs

Organism: Equus caballus

Library:

Name: unspecified

Instrument: Illumina NovaSeq 6000

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Runs: 1 run, 721.3M spots, 217.8G bases, 64Gb

Run	# of Spots	# of Bases	Size	Published
ERR3888647	721,250,395	217.8G	64Gb	2020-09-02

ID:: 11767332

SRA

Sequence Read Archive

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