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

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

Summary: 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) b...

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Bibliographic Details
Main Authors: Mingyi Yang, Omer Ali, Magnar Bjørås, Junbai Wang
Format: Article
Language:English
Published: Elsevier 2023-08-01
Series:iScience
Subjects:
Biological sciences
Bioinformatics
Biocomputational method
Omics
Biological sciences tools
Online Access:http://www.sciencedirect.com/science/article/pii/S2589004223013433

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http://www.sciencedirect.com/science/article/pii/S2589004223013433

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