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Music2identifying mutational significance in cancer genomes
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AgfusionPython package to annotate and visualize gene fusions.
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Sv CallersSnakemake-based workflow for detecting structural variants in WGS data
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CbioportalcBioPortal for Cancer Genomics
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civic-clientWeb client for CIViC: Clinical Interpretations of Variants in Cancer
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revolverREVOLVER - Repeated Evolution in Cancer
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pathway-mapperPathwayMapper: An interactive and collaborative graphical curation tool for cancer pathways
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SigProfilerPlottingSigProfilerPlotting provides a standard tool for displaying all types of mutational signatures as well as all types of mutational patterns in cancer genomes. The tool seamlessly integrates with other SigProfiler tools.
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TeamTeriGenomics using open source tools, running on GCP or AWS
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cpsrCancer Predisposition Sequencing Reporter (CPSR)
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genome-nexusBackend server for Genome Nexus
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mauiMulti-omics Autoencoder Integration: Deep learning-based heterogenous data analysis toolkit
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IMPACT-PipelineFramework to process and call somatic variation from NGS dataset generated using MSK-IMPACT assay
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orchidA novel management, annotation, and machine learning framework for analyzing cancer mutations
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SigProfilerSimulatorSigProfilerSimulator allows realistic simulations of mutational patterns and mutational signatures in cancer genomes. The tool can be used to simulate signatures of single point mutations, double point mutations, and insertion/deletions. Further, the tool makes use of SigProfilerMatrixGenerator and SigProfilerPlotting.
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civic-serverBackend Server for CIViC Project
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SigProfilerMatrixGeneratorSigProfilerMatrixGenerator creates mutational matrices for all types of somatic mutations. It allows downsizing the generated mutations only to parts for the genome (e.g., exome or a custom BED file). The tool seamlessly integrates with other SigProfiler tools.
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deTiNDeTiN is designed to measure tumor-in-normal contamination and improve somatic variant detection sensitivity when using a contaminated matched control.
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SCICoNESingle-cell copy number calling and event history reconstruction.
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cacaoCallable Cancer Loci - assessment of sequencing coverage for actionable and pathogenic loci in cancer
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Variants2NeoantigenA neoantigen calling pipeline begins from variants record file (MAF) (Not maintain now)
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MaftoolsSummarize, Analyze and Visualize MAF files from TCGA or in house studies.
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DellyDELLY2: Structural variant discovery by integrated paired-end and split-read analysis
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Awesome Cancer Variant DatabasesA community-maintained repository of cancer clinical knowledge bases and databases focused on cancer variants.
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IdeogramChromosome visualization for the web
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PcgrPersonal Cancer Genome Reporter (PCGR)
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LollipopsLollipop-style mutation diagrams for annotating genetic variations.
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