Back to search

Article

Background splicing and genetic disease

2020-10-15

Abstract excerpt

We report that low level background splicing by normal genes can be used to predict the likely effect of splicing mutations upon cryptic splice site activation and exon skipping, with emphasis on the DBASS databases, BRCA1, BRCA2 and DMD. In addition we show that background RNA splice sites are also involved in pseudoexon formation, recursive splicing and aberrant splicing in cancer. We discuss how background spli...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
50271646-7e33-5c3e-8463-80cff4880b88
DOI
10.21203/rs.3.rs-92665/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Background splicing and genetic diseaseDOI 10.21203/rs.3.rs-92665/v1
Select a neighboring publication to make it the new centre.