CLISGen: A Comprehensive Resource of SNP Genotypes for Human Cell Lines

Selecting cell lines with specific Single Nucleotide Polymorphism (SNP) genotypes is a critical bottleneck in functional genomics, often requiring advanced bioinformatic skills. To address this, we developed CLISGen (Cell LInes SNP Genotypes), a database with a user-friendly web application that simplifies access to SNP genotypes in over 1000 cancer cell lines from the Cancer Cell Line Encyclopedia. CLISGen integrates and harmonizes data from Whole-Genome, Whole-Exome, and RNA sequencing, enriching it with contextual information like copy number alterations and genetic ancestry. The platform allows users to search for specific variants or variants in specific genes or genomic regions and filter results by tissue type or data quality, providing intuitive graphical and tabular outputs. By eliminating a major experimental bottleneck, CLISGen offers researchers a powerful resource to efficiently select suitable cell models for studying the link between genetic variation and cancer. CLISGen is freely available at https://bcglab.cibio.unitn.it/clisgen.

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Publication Details

Journal
Journal of Molecular Biology
Published
2026-02-01
DOI
https://doi.org/10.1016/j.jmb.2026.169681
Primary Topic
Cancer Genomics and Diagnostics
Type
article
Field-Weighted Citation Impact
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article

CLISGen: A Comprehensive Resource of SNP Genotypes for Human Cell Lines

Davide Dalfovo, Alessandro Romanel, Matteo Marchesin
Journal of Molecular Biology
Cancer Genomics and Diagnostics
article

CLISGen: A Comprehensive Resource of SNP Genotypes for Human Cell Lines

Davide Dalfovo, Alessandro Romanel, Matteo Marchesin
article en

Abstract

Selecting cell lines with specific Single Nucleotide Polymorphism (SNP) genotypes is a critical bottleneck in functional genomics, often requiring advanced bioinformatic skills. To address this, we developed CLISGen (Cell LInes SNP Genotypes), a database with a user-friendly web application that simplifies access to SNP genotypes in over 1000 cancer cell lines from the Cancer Cell Line Encyclopedia. CLISGen integrates and harmonizes data from Whole-Genome, Whole-Exome, and RNA sequencing, enriching it with contextual information like copy number alterations and genetic ancestry. The platform allows users to search for specific variants or variants in specific genes or genomic regions and filter results by tissue type or data quality, providing intuitive graphical and tabular outputs. By eliminating a major experimental bottleneck, CLISGen offers researchers a powerful resource to efficiently select suitable cell models for studying the link between genetic variation and cancer. CLISGen is freely available at https://bcglab.cibio.unitn.it/clisgen.

Journal of Molecular Biology
University of Padua (IT), University of Trento (IT)
Quality Education
Openalex Percentile: Top 67%
Cancer Genomics and Diagnostics
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