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DRX424657: Illumina paired end sequencing of SAMD00573998
1 ILLUMINA (Illumina NovaSeq 6000) run: 320.9M spots, 96.9G bases, 36.2Gb downloads

Submitted by: LRC
Study: Rare and common variant discovery by whole-genome sequencing of 101 Thoroughbred racehorses
PRJDB15140 • DRP009556 • All experiments • All runs
show Abstracthide Abstract
The Thoroughbred breed was formed by crossing Oriental horse breeds and British native horses and is currently used in horseracing worldwide. In this project, we constructed a single-nucleotide variant (SNV) database using data from 101 Thoroughbred racehorses. The number of SNVs detected in individual horses ranged from 4.8 to 5.3 million.
Sample: whole genome sequence of LRC_090
SAMD00573998 • DRS278524 • All experiments • All runs
Organism: Equus caballus
Library:
Name: Library_LRC_090
Instrument: Illumina NovaSeq 6000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: TruSeq DNA PCR-free Library
Pipeline: show...hide...
StepPrev Step
1NIL
Runs: 1 run, 320.9M spots, 96.9G bases, 36.2Gb
Run# of Spots# of BasesSizePublished
DRR439483320,945,81996.9G36.2Gb2023-02-03

ID:
26492858

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