scVMAP: a comprehensive platform for integrating single-cell chromatin accessibility regions with causal variants.
第一作者:
Zheng-Min,Yu
第一单位:
The First Affiliated Hospital & Hunan Provincial Key Laboratory of Multi-omics and Artificial Intelligence of Cardiovascular Diseases, Hengyang Medical School, University of South China, Hengyang, Hunan 421001, China.;School of Computer, University of South China, Hengyang, Hunan 421001, China.
作者:
医学主题词
单细胞分析(Single-Cell Analysis);染色质(Chromatin);人类(Humans);软件(Software);转录因子(Transcription Factors);高通量核苷酸序列分析(High-Throughput Nucleotide Sequencing);全基因组关联研究(Genome-Wide Association Study);数据库, 遗传学(Databases, Genetic);遗传变异(Genetic Variation);多态性, 单核苷酸(Polymorphism, Single Nucleotide);数量性状基因座位(Quantitative Trait Loci);动物(Animals);转座酶类(Transposases)
DOI
10.1093/nar/gkaf1112
PMID
41171141
发布时间
2026-01-18
- 浏览0
Nucleic acids research
D1270-D1280页
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