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    • Nextflow pipeline for predicting variant stability across reference genome builds.
      R
      0001Updated Aug 19, 2025Aug 19, 2025
    • Nextflow pipeline to call germline short variants using GATK
      Nextflow
      11212Updated Aug 19, 2025Aug 19, 2025
    • Set of commonly used Nextflow modules
      Nextflow
      0091Updated Aug 19, 2025Aug 19, 2025
    • Nextflow pipeline to identify the somatic single nucleotide variants (sSNVs) by comparing a pair of tumor/normal samples.
      Nextflow
      26363Updated Aug 18, 2025Aug 18, 2025
    • Shell
      0111Updated Aug 18, 2025Aug 18, 2025
    • Nextflow pipeline to align paired DNA FASTQs and sort, mark duplicates, and index resulting alignment
      Nextflow
      14252Updated Aug 18, 2025Aug 18, 2025
    • Nextflow pipeline to generate sample level QC data from BAM files
      Groovy
      00172Updated Aug 18, 2025Aug 18, 2025
    • Nextflow pipeline to calculate mitochondrial DNA copy number
      Groovy
      0000Updated Aug 18, 2025Aug 18, 2025
    • Nextflow pipeline to call germline structural variants and copy number variants using DELLY and Manta
      R
      12112Updated Aug 18, 2025Aug 18, 2025
    • CLI to automate Nextflow pipeline testing
      Python
      112161Updated Aug 18, 2025Aug 18, 2025
    • Python
      0072Updated Aug 18, 2025Aug 18, 2025
    • Nextflow pipeline to perform Indel Realignment and Base Quality Score Recalibration
      Nextflow
      11145Updated Aug 15, 2025Aug 15, 2025
    • Nextflow pipeline to call somatic structural variants using DELLY, GRIDSS2 and Manta
      Nextflow
      02172Updated Aug 15, 2025Aug 15, 2025
    • Nextflow pipeline to detect mitochondrial SNV from normal or tumor BAMs or CRAMs: extracts and remaps mitochondorial reads then calls variants
      Nextflow
      01183Updated Aug 13, 2025Aug 13, 2025
    • GitHub reusable workflows to manage the release process
      Python
      0000Updated Aug 13, 2025Aug 13, 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
      110360Updated Aug 13, 2025Aug 13, 2025
    • An Action to automatically build and push images to the GitHub Container registry. Includes automatic building of images for development.
      JavaScript
      0030Updated Aug 13, 2025Aug 13, 2025
    • Nextflow pipeline to calculate read-depth related stats for targeted sequencing experiments
      Nextflow
      00102Updated Aug 12, 2025Aug 12, 2025
    • Multi-Omics Peptide Generator
      Python
      423271Updated Aug 11, 2025Aug 11, 2025
    • Nextflow pipeline to generate custom databases of non-canonical peptides for proteogenomic analysis
      Nextflow
      2232Updated Aug 11, 2025Aug 11, 2025
    • GitHub composite Action to perform static code analysis
      Python
      0010Updated Aug 11, 2025Aug 11, 2025
    • Publication Quality Phylogenetic Tree Plots
      R
      02202Updated Aug 11, 2025Aug 11, 2025
    • Functions to Create Publication-Quality Plots
      R
      415612Updated Aug 11, 2025Aug 11, 2025
    • 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
      0080Updated Aug 7, 2025Aug 7, 2025
    • Docker repository for Delly
      Dockerfile
      0000Updated Jul 31, 2025Jul 31, 2025
    • Dockerfile
      0000Updated Jul 25, 2025Jul 25, 2025
    • Docker repository for BWA-MEM2 and SAMtools
      Dockerfile
      0011Updated Jul 25, 2025Jul 25, 2025
    • Automated scoring system for the SMC-Het Challenge
      Python
      0100Updated Jul 14, 2025Jul 14, 2025
    • Ligare

      Public
      Python
      01162Updated Jul 9, 2025Jul 9, 2025
    • R
      0141Updated Jul 1, 2025Jul 1, 2025