ISVASE: identification of sequence variant associated with splicing event using RNA-seq data.

Hasan Awad AljohiWanfei LiuQiang LinJun YuSongnian Hu

Published in: BMC bioinformatics (2017)

ISVASE is useful for researchers interested in sequence variants (DNA mutation and/or RNA editing) associated with splicing events. The package is freely available at https://sourceforge.net/projects/isvase/ .

Keyphrases

rna seq
single cell
crispr cas
circulating tumor
nucleic acid
electronic health record
copy number
cell free
quality improvement
amino acid
big data
dna methylation
bioinformatics analysis
data analysis
circulating tumor cells
deep learning