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• W4283729263 abstract "The usage of expressed somatic mutations may have a unique advantage in identifying active cancer driver mutations. However, accurately calling mutations from RNA-seq data is difficult due to confounding factors such as RNA-editing, reverse transcription, and gap alignment. In the present study, we proposed a framework (named RNA-SSNV, https://github.com/pmglab/RNA-SSNV) to call somatic single nucleotide variants (SSNV) from tumor bulk RNA-seq data. Based on a comprehensive multi-filtering strategy and a machine-learning classification model trained with comprehensively curated features, RNA-SSNV achieved the best precision-recall rate (0.880-0.884) in a testing dataset and robustly retained 0.94 AUC for the precision-recall curve in three validation adult-based TCGA (The Cancer Genome Atlas) datasets. We further showed that the somatic mutations called by RNA-SSNV tended to have a higher functional impact and therapeutic power in known driver genes. Furthermore, VAF (variant allele fraction) analysis revealed that subclonal harboring expressed mutations had evolutional selection advantage and RNA had higher detection power to rescue DNA-omitted mutations. In sum, RNA-SSNV will be a useful approach to accurately call expressed somatic mutations for a more insightful analysis of cancer drive genes and carcinogenic mechanisms." @default.
• W4283729263 created "2022-07-01" @default.
• W4283729263 creator A5015753176 @default.
• W4283729263 creator A5030446906 @default.
• W4283729263 creator A5040633212 @default.
• W4283729263 date "2022-06-30" @default.
• W4283729263 modified "2023-09-30" @default.
• W4283729263 title "RNA-SSNV: A Reliable Somatic Single Nucleotide Variant Identification Framework for Bulk RNA-Seq Data" @default.
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• W4283729263 doi "https://doi.org/10.3389/fgene.2022.865313" @default.

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