BAYSIC: a Bayesian method for combining sets of genome variants with improved specificity and sensitivity | BMC Bioinformatics | Full Text
Available resources and challenges for the clinical annotation of somatic variations - Dumur - 2014 - Cancer Cytopathology - Wiley Online Library
Preparation for Somatic Mutation Annotator
Cancer Genomics Research — Resources and Databases | Medium
Frontiers | DeteX: A highly accurate software for detecting SNV and InDel in single and paired NGS data in cancer research
BRB-SeqTools
NeoMutate: an ensemble machine learning framework for the prediction of somatic mutations in cancer | BMC Medical Genomics | Full Text
Translating COSMIC's gold standard data into actionable insights - Bioinformatics Software | QIAGEN Digital Insights
VCF file from COSMIC · Issue #3 · zstephens/neat-genreads · GitHub
ICGC: The Next Generation Cancer Mutation Database Now Available | The Golden Helix Blog
COSMIC: somatic cancer genetics at high-resolution. - Abstract - Europe PMC
Mutation Details from COSMIC Details for BRAF Tissue Mutations (% of... | Download Table
Variant Recoder
COSMIC v91 release coming soon
A practical framework RNMF for exploring the association between mutational signatures and genes using gene cumulative contribution abundance - Li - 2022 - Cancer Medicine - Wiley Online Library
Reporting workflow for somatic variants. All variants outputs from the... | Download Scientific Diagram
Topography of mutational signatures in human cancer - ScienceDirect
Introduction
COSMIC v91 release coming soon
ApoCanD: Database of human apoptotic proteins in the context of cancer | Scientific Reports
Download Files
MutSpec: a Galaxy toolbox for streamlined analyses of somatic mutation spectra in human and mouse cancer genomes | BMC Bioinformatics | Full Text
