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    • A bioinformatics best-practice analysis pipeline for calling structural variants (SVs), copy number variants (CNVs) and repeat region expansions (RREs) from short DNA reads
      Nextflow
      MIT License
      219172Updated Feb 13, 2025Feb 13, 2025
    • Preprocessing workflow for sequencing data at CMGG
      Nextflow
      MIT License
      2340Updated Feb 11, 2025Feb 11, 2025
    • germline

      Public
      A nextflow pipeline for calling and annotating small germline variants from short DNA reads for WES and WGS data
      Nextflow
      MIT License
      18111Updated Feb 4, 2025Feb 4, 2025
    • CMGG Sampletracking workflow
      Nextflow
      MIT License
      0060Updated Jan 30, 2025Jan 30, 2025
    • exomecnv

      Public
      A nextflow pipeline for calling exome CNVs
      Nextflow
      MIT License
      2941Updated Jan 23, 2025Jan 23, 2025
    • configs

      Public
      Nextflow config files
      MIT License
      1000Updated Jan 16, 2025Jan 16, 2025
    • Test datasets for unit tests with the nf-cmgg pipelines
      MIT License
      1000Updated Jan 14, 2025Jan 14, 2025
    • A nextflow pipeline for creating references for WisecondorX
      Nextflow
      MIT License
      1000Updated Apr 24, 2024Apr 24, 2024
    • The repository used at the Beginner Nextflow course in february 2024
      Nextflow
      MIT License
      1500Updated Feb 7, 2024Feb 7, 2024
    • qdnaseq

      Public
      A Nextflow pipeline to create qDNAseq bin annotations
      Nextflow
      MIT License
      0000Updated Sep 7, 2023Sep 7, 2023