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    • Variant calling pipeline for RNAseq aligned data
      Nextflow
      0000Updated Aug 11, 2025Aug 11, 2025
    • nl-wgs_wf

      Public
      Whole genome sequecing pipeline for germline short-read data
      Nextflow
      0020Updated Aug 7, 2025Aug 7, 2025
    • wgs_qc_wf

      Public
      Workflow used to check QC for WGS data
      Nextflow
      0000Updated Jun 5, 2025Jun 5, 2025
    • RNA-seq for rare diseases pipeline using nextflow
      Nextflow
      0100Updated Jun 5, 2025Jun 5, 2025
    • A tool for estimating repeat sizes
      C++
      53000Updated Dec 11, 2024Dec 11, 2024
    • Nextflow pipeline to call germline short variants using GATK
      Nextflow
      1000Updated Nov 2, 2024Nov 2, 2024
    • Archive with samples data available and doctor information
      R
      0000Updated Oct 21, 2024Oct 21, 2024
    • Website for Stanley Nelson Laboratory from UCLA at human genetics department
      SCSS
      0000Updated Oct 10, 2024Oct 10, 2024
    • Nextflow pipeline to call germline structural variants and copy number variants using DELLY and Manta
      Nextflow
      1000Updated May 21, 2024May 21, 2024
    • Nextflow pipeline to align paired DNA FASTQs and sort, mark duplicates, and index resulting alignment
      Nextflow
      1000Updated May 21, 2024May 21, 2024
    • Nextflow pipeline to perform Indel Realignment and Base Quality Score Recalibration
      Nextflow
      1000Updated May 21, 2024May 21, 2024