Cargando…
RegVar: Tissue-specific Prioritization of Non-coding Regulatory Variants
Non-coding genomic variants constitute the majority of trait-associated genome variations; however, the identification of functional non-coding variants is still a challenge in human genetics, and a method for systematically assessing the impact of regulatory variants on gene expression and linking...
Autores principales: | Lu, Hao, Ma, Luyu, Quan, Cheng, Li, Lei, Lu, Yiming, Zhou, Gangqiao, Zhang, Chenggang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10626172/ https://www.ncbi.nlm.nih.gov/pubmed/34973416 http://dx.doi.org/10.1016/j.gpb.2021.08.011 |
Ejemplares similares
-
Prioritization of regulatory variants with tissue-specific function in the non-coding regions of human genome
por: Dong, Shengcheng, et al.
Publicado: (2021) -
CellRegMap: a statistical framework for mapping context‐specific regulatory variants using scRNA‐seq
por: Cuomo, Anna S E, et al.
Publicado: (2022) -
regBase: whole genome base-wise aggregation and functional prediction for human non-coding regulatory variants
por: Zhang, Shijie, et al.
Publicado: (2019) -
iRegNet3D: three-dimensional integrated regulatory network for the genomic analysis of coding and non-coding disease mutations
por: Liang, Siqi, et al.
Publicado: (2017) -
FunSeq2: a framework for prioritizing noncoding regulatory variants in cancer
por: Fu, Yao, et al.
Publicado: (2014)