官方服务：
资源简介：
human resequencing Genome sequencing
应用场景：
创建时间：
2018-02-12
相关数据集
Overlapping CNV segments in familial CoA with candidate gene.
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
NWD841275.freeze5.v1.vcf.gz
TOPMed: NWD841275.freeze5.v1.vcf.gz File: VCF file
DataCite Commons2020-09-20 更新40
Supplementary data of Figures (S1) and Tables (S1 & S2)
Figure S1. Comparison of early flower mutant recovered from irradiated PLBs at 10 Gy dose with the flower of ‘Emma White’ mother plant Table S1: Mean DNA intensity and nuclei
Zenodo2022-09-14 更新20
HipSci supporting data for publication "Common genetic variation drives molecular heterogeneity in human iPSCs"
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
JinbSamgNippIndiKitKasal.filtered.miss10.vcf.gz
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
