Abstract

Barley (Hordeum vulgare L.) is one of the first domesticated grain crops and represents the fourth most important cereal source for human and animal consumption. BarleyVarDB is a database of barley genomic variation. It can be publicly accessible through the website at http://146.118.64.11/BarleyVar. This database mainly provides three sets of information. First, there are 57 754 224 single nuclear polymorphisms (SNPs) and 3 600 663 insertions or deletions (InDels) included in BarleyVarDB, which were identified from high-coverage whole genome sequencing of 21 barley germplasm, including 8 wild barley accessions from 3 barley evolutionary original centers and 13 barley landraces from different continents. Second, it uses the latest barley genome reference and its annotation information publicly accessible, which has been achieved by the International Barley Genome Sequencing Consortium (IBSC). Third, 522 212 whole genome-wide microsatellites/simple sequence repeats (SSRs) were also included in this database, which were identified in the reference barley pseudo-molecular genome sequence. Additionally, several useful web-based applications are provided including JBrowse, BLAST and Primer3. Users can design PCR primers to asses polymorphic variants deposited in this database and use a user-friendly interface for accessing the barley reference genome. We envisage that the BarleyVarDB will benefit the barley genetic research community by providing access to all publicly available barley genomic variation information and barley reference genome as well as providing them with an ultra-high density of SNP and InDel markers for molecular breeding and identification of functional genes with important agronomic traits in barley. Database URL: http://146.118.64.11/BarleyVar

Highlights

  • Single nuclear polymorphisms (SNPs) and insertions or deletions (InDels) are the two most common types of genetic variations among living organisms

  • A comprehensive database of barley genomic variation is in an urgent need for the barley genomic research community to share and make good use of the genomic variation information exploited by different research groups

  • 57 754 224 single nuclear polymorphisms (SNPs) and 3 600 663 InDels identified from high coverage whole genome sequencing (∼40X) of 20 diverse barley germplasms representing wild barley accessions from 3 widely accepted barley evolutionary original centers and cultivar barley accessions from different continents

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Summary

Introduction

Single nuclear polymorphisms (SNPs) and insertions or deletions (InDels) are the two most common types of genetic variations among living organisms. We constructed a comprehensive database specializing in barley genomic variation and designated it as BarleyVarDB. 57 754 224 SNPs and 3 600 663 InDels identified from high coverage whole genome sequencing (∼40X) of 20 diverse barley germplasms representing wild barley accessions from 3 widely accepted barley evolutionary original centers and cultivar barley accessions from different continents.

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