Author

Mischan Vali-Pour

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

Biology Disciplines

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Signature Assays, Organisms & Methods

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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

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2 top collaborators · 1 mutual co-author link

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1 shared paperGenomics

Ben LehnerORCID

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1 paper

Recent·Most cited

GenomicsbioRxivPreprintNov 14, 2021

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.

2 citations

humanwhole-exome sequencing

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