Identifying functional regulatory mutation blocks by integrating genome sequencing and transcriptome data

Millions of single nucleotide variants (SNVs) exist in the human genome; however, it remains challenging to identify functional SNVs associated with diseases. We propose a non-encoding SNVs analysis tool bpb3, BayesPI-BAR version 3, aiming to identify the functional mutation blocks (FMBs) by integra...

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Detalles Bibliográficos
Autores principales: Yang, Mingyi, Ali, Omer, Bjørås, Magnar, Wang, Junbai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371843/
https://www.ncbi.nlm.nih.gov/pubmed/37520692
http://dx.doi.org/10.1016/j.isci.2023.107266

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371843/
https://www.ncbi.nlm.nih.gov/pubmed/37520692
http://dx.doi.org/10.1016/j.isci.2023.107266

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