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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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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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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Sv CallersSnakemake-based workflow for detecting structural variants in WGS data
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Somalierfast sample-swap and relatedness checks on BAMs/CRAMs/VCFs/GVCFs... "like damn that is one smart wine guy"
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2020plusClassifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests
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PygenoPersonalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
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pathway-mapperPathwayMapper: An interactive and collaborative graphical curation tool for cancer pathways
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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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TeamTeriGenomics using open source tools, running on GCP or AWS
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epivizEpiViz is a scientific information visualization tool for genetic and epigenetic data, used to aid in the exploration and understanding of correlations between various genome features.
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orfipyFast and flexible ORF finder
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motifmatchrFast motif matching in R
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perbasePer-base per-nucleotide depth analysis
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CATTAn ultra-sensitive and precise tool for characterizing T cell CDR3 sequences in TCR-seq and RNA-seq data.
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SVCollectorMethod to optimally select samples for validation and resequencing
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geneviewGenomics data visualization in Python by using matplotlib.
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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calN50Compute N50/NG50 and auN/auNG
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polyRADGenotype Calling with Uncertainty from Sequencing Data in Polyploids 🍌🍓🥔🍠🥝
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flexidotHighly customizable, ambiguity-aware dotplots for visual sequence analyses
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CENTIPEDE.tutorial🐛 How to use CENTIPEDE to determine if a transcription factor is bound.
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referenceseekerRapid determination of appropriate reference genomes.
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crazydocRead DNA sequences from colourful Microsoft Word documents
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OpenGene.jl(No maintenance) OpenGene, core libraries for NGS data analysis and bioinformatics in Julia
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calourexploratory and interactive microbiome analyses based on heatmaps
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dna-sculpture3D printed sculpture of a DNA molecule, showing my own genome
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chromapFast alignment and preprocessing of chromatin profiles
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bystroBystro genetic analysis (annotation, filtering, statistics)
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matamMapping-Assisted Targeted-Assembly for Metagenomics
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biskitA Python platform for Structural Bioinformatics
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reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
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mulledMulled - Automatized Containerized Software Repository
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hotmapWebGL Heatmap Viewer for Big Data and Bioinformatics
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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BioKEENA computational library for learning and evaluating biological knowledge graph embeddings
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mviewMView extracts and reformats the results of a sequence database search or multiple alignment.
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revolverREVOLVER - Repeated Evolution in Cancer
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awesome-small-molecule-mlA curated list of resources for machine learning for small-molecule drug discovery
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ccsCCS: Generate Highly Accurate Single-Molecule Consensus Reads (HiFi Reads)
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awesome-geneticsA curated list of awesome bioinformatics software.
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CAFE5Version 5 of the CAFE phylogenetics software
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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CoNekTCoNekT (short for Co-expression Network Toolkit) is a platform to browse co-expression data and enable cross-species comparisons.
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gene-oracleFeature extraction algorithm for genomic data
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GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
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catchA package for designing compact and comprehensive capture probe sets.
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tftargets🎯 Human transcription factor target genes.
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MSFraggerUltrafast, comprehensive peptide identification for mass spectrometry–based proteomics
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TypeTEGenotyping of segregating mobile elements insertions
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StackedDAEStacked Denoising AutoEncoder based on TensorFlow
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nPhasePloidy agnostic phasing pipeline and algorithm
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bio toolsUseful bioinformatic scripts
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atroposAn NGS read trimming tool that is specific, sensitive, and speedy. (production)
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block-alignerSIMD-accelerated library for computing global and X-drop affine gap penalty sequence-to-sequence or sequence-to-profile alignments using an adaptive block-based algorithm.
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