SNP MI 30%

Dryad2015-01-01 更新2026-04-13 收录

遗传变异分析

基因型插补

数据链接：

http://datadryad.org/resource/doi:10.5061/dryad.8kb37/2 数据链接链接失效反馈

官方服务：

资源简介：

Genotyping-by-sequence imputated SNP file with 30% missing data using the mean imputation method

创建时间：

2015-01-01

Overlapping CNV segments in familial CoA with candidate gene.

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

Comparison of allele counts between AA cases and controls for different variant classes.

遗传变异分析

群体遗传学

Comparison of allele counts between AA cases and controls for different variant classes.

NIAID Data Ecosystem50

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

HipSci supporting data for publication "Common genetic variation drives molecular heterogeneity in human iPSCs"

干细胞分子异质性

遗传变异分析

The Human Induced Pluripotent Stem Cells Initiative (HipSci) is generating a large, high-quality reference panel of human IPSC lines. This BioStudies submission comprises only the data used in the an

NIAID Data Ecosystem60

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