Author

Mischan Vali-Pour

Universitat Pompeu FabraORCID 0000-0002-9014-1960Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Ben LehneriD· 1 shared Fran SupekiD· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

2 top collaborators · 1 mutual co-author link

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

1 shared paperGenomics

Ben LehnerORCID

Mutual co-authors in cluster

Author profile →

1 paper

Recent·Most cited

The impact of rare germline variants on human somatic mutation processes

Mischan Vali-Pour, Ben Lehner, Fran Supek

This study identifies 207 associations between rare germline variants and somatic mutational processes in cancer genomes, revealing novel genes influencing DNA repair and mutation signatures.

bioRxiv · Nov 14, 2021 · PreprintGenomics