Unknown

Dataset Information

0

RiceVarMap: a comprehensive database of rice genomic variations.


ABSTRACT: Rice Variation Map (RiceVarMap, http:/ricevarmap.ncpgr.cn) is a database of rice genomic variations. The database provides comprehensive information of 6,551,358 single nucleotide polymorphisms (SNPs) and 1,214,627 insertions/deletions (INDELs) identified from sequencing data of 1479 rice accessions. The SNP genotypes of all accessions were imputed and evaluated, resulting in an overall missing data rate of 0.42% and an estimated accuracy greater than 99%. The SNP/INDEL genotypes of all accessions are available for online query and download. Users can search SNPs/INDELs by identifiers of the SNPs/INDELs, genomic regions, gene identifiers and keywords of gene annotation. Allele frequencies within various subpopulations and the effects of the variation that may alter the protein sequence of a gene are also listed for each SNP/INDEL. The database also provides geographical details and phenotype images for various rice accessions. In particular, the database provides tools to construct haplotype networks and design PCR-primers by taking into account surrounding known genomic variations. These data and tools are highly useful for exploring genetic variations and evolution studies of rice and other species.

SUBMITTER: Zhao H 

PROVIDER: S-EPMC4384008 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

altmetric image

Publications

RiceVarMap: a comprehensive database of rice genomic variations.

Zhao Hu H   Yao Wen W   Ouyang Yidan Y   Yang Wanneng W   Wang Gongwei G   Lian Xingming X   Xing Yongzhong Y   Chen Lingling L   Xie Weibo W  

Nucleic acids research 20141001 Database issue


Rice Variation Map (RiceVarMap, http:/ricevarmap.ncpgr.cn) is a database of rice genomic variations. The database provides comprehensive information of 6,551,358 single nucleotide polymorphisms (SNPs) and 1,214,627 insertions/deletions (INDELs) identified from sequencing data of 1479 rice accessions. The SNP genotypes of all accessions were imputed and evaluated, resulting in an overall missing data rate of 0.42% and an estimated accuracy greater than 99%. The SNP/INDEL genotypes of all accessio  ...[more]

Similar Datasets

| S-EPMC7145649 | biostudies-literature
| S-EPMC2721851 | biostudies-literature
| S-EPMC8988285 | biostudies-literature
| S-EPMC8131054 | biostudies-literature
| S-EPMC8724205 | biostudies-literature
| S-EPMC3627721 | biostudies-literature
| S-EPMC10851451 | biostudies-literature
| S-EPMC6791890 | biostudies-literature
| S-EPMC9632082 | biostudies-literature