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    • Publication Quality Phylogenetic Tree Plots
      R
      02202Updated Jan 23, 2026Jan 23, 2026
    • Utilities for matching a polygenic score coordinate file to a VCF input and the subsequent calculation of the provided polygenic score in each individual.
      R
      0180Updated Jan 23, 2026Jan 23, 2026
    • Helper Functions to Normalize NanoString CNV Data
      R
      0001Updated Jan 23, 2026Jan 23, 2026
    • R
      0141Updated Jan 23, 2026Jan 23, 2026
    • Detection of Kataegis
      R
      0010Updated Jan 23, 2026Jan 23, 2026
    • Aggregation of QC metrics and outlier nomination for multi-sample studies
      R
      0151Updated Jan 23, 2026Jan 23, 2026
    • HistogramZoo - A set of methods for histogram segmentation and characterization
      R
      03350Updated Jan 22, 2026Jan 22, 2026
    • Functions to Create Publication-Quality Plots
      R
      416612Updated Jan 21, 2026Jan 21, 2026
    • Generate High-Resolution Venn and Euler Plots
      R
      2762Updated Jan 14, 2026Jan 14, 2026
    • Ligare

      Public
      Python
      01167Updated Jan 8, 2026Jan 8, 2026
    • Shell
      1112Updated Dec 22, 2025Dec 22, 2025
    • GitHub reusable workflows to manage the release process
      Python
      1003Updated Dec 15, 2025Dec 15, 2025
    • CLI to automate Nextflow pipeline testing
      Python
      212163Updated Dec 15, 2025Dec 15, 2025
    • Nextflow pipeline for predicting variant stability across reference genome builds.
      R
      1002Updated Nov 24, 2025Nov 24, 2025
    • An Action to automatically build and push images to the GitHub Container registry. Includes automatic building of images for development.
      JavaScript
      2033Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to identify the somatic single nucleotide variants (sSNVs) by comparing a pair of tumor/normal samples.
      Nextflow
      36365Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to call germline short variants using GATK
      Nextflow
      21214Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to convert BAM to FASTQ, align, perform QC, assess targeted coverage, call gSNP, call sSNV, call mtSNV, call SVs, call sCNA, and perform subclonal reconstruction
      Groovy
      111351Updated Nov 24, 2025Nov 24, 2025
    • GitHub composite Action to perform static code analysis
      Python
      1012Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to call somatic structural variants using DELLY, GRIDSS2 and Manta
      Nextflow
      12152Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to align paired DNA FASTQs and sort, mark duplicates, and index resulting alignment
      Nextflow
      24263Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to call germline structural variants and copy number variants using DELLY and Manta
      R
      22112Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to calculate mitochondrial DNA copy number
      Groovy
      0002Updated Nov 24, 2025Nov 24, 2025
    • Nextflow pipeline to generate sample level QC data from BAM files
      Groovy
      00173Updated Nov 24, 2025Nov 24, 2025
    • Multi-Omics Peptide Generator
      Python
      530271Updated Nov 6, 2025Nov 6, 2025
    • Python
      1065Updated Oct 27, 2025Oct 27, 2025
    • R
      0011Updated Oct 17, 2025Oct 17, 2025
    • R
      0100Updated Oct 13, 2025Oct 13, 2025
    • A transcriptomic compendium for a variety of current and upcoming models used to study Prostate cancer.
      R
      00113Updated Sep 8, 2025Sep 8, 2025
    • Nextflow pipeline to perform Indel Realignment and Base Quality Score Recalibration
      Nextflow
      21142Updated Sep 2, 2025Sep 2, 2025