ClairS - a deep-learning method for long-read somatic small variant calling
ClairS-TO - a deep-learning method for tumor-only somatic variant calling
Bioinformatic Analysis pipeLine for SomAtic Mutations In Cancer
Snakemake workflow for somatic mutation detection without matched normal samples
Galaxy Tool Shed repositories maintained and developed by the Morin Lab.
Pipeline to call SNV's with 4 tools (VarDict, LoFreq, Mutect2 & SiNVICT)
Detects hotspot regions for somatic mutations in 3D protein structures
a Nextflow SNV calling and annotation pipeline based on DKFZ-ODCF/SNVCallingWorkflow
This page is reserved for NextFlow based Indell Calling Workflow (with Platypus) from DKFZ
Depository for Bioinformatics Master Project HT2022-VT2023
AI-based prediction of driver mutations
Snakemake Pipeline for the Analyses of ChIP-seq data in Cancer samples
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