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imputed-seq-genotypes-12k-Chr5.31060000-32060000.vcf

DataONE2017-12-15 更新2024-06-26 收录

基因型推断

遗传变异分析

数据链接：

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资源简介：

Imputed genotypes for variants within 1Mbp of the Chr5:31.56 LC QTL, for 12,000 animals.

应用场景：

创建时间：

2017-12-15

遗传变异分析

主动脉疾病研究

Seven overlapping CNVs shared in >4 individuals with CoA were identified. The chromosome 21 CNV locus was present in all familial CoA cases. It contains TRPM2, which was also identified in the sporadi

NIAID Data Ecosystem100

Synonymous variants in enhancer and splicing regions identified in families co-segregating with ET based on MM-KBAC analysis of rare variants.

遗传变异分析

原发性震颤致病机制

Synonymous variants in enhancer and splicing regions identified in families co-segregating with ET based on MM-KBAC analysis of rare variants.

NIAID Data Ecosystem40

JinbSamgNippIndiKitKasal.filtered.miss10.vcf.gz

水稻转录组学

遗传变异分析

Filtered variant call format (VCF) data of Jinbuol (JBO, female), Samgwang (SG, male), two RIL individuals (JSRIL1 and JSRIL2), Nipponbare1, IndicaHR12, Kitaake, and Kasalath using resequencing data p

DataCite Commons2024-11-11 更新30

Distribution of SNPs and InDels on rice chromosomes.

水稻转录组学

遗传变异分析

Distribution of SNPs and InDels on rice chromosomes.

Figshare2015-12-02 更新40

NWD841275.freeze5.v1.vcf.gz

遗传变异分析

精准医疗基因组学

TOPMed: NWD841275.freeze5.v1.vcf.gz File: VCF file

DataCite Commons2020-09-20 更新40