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RCollins13 (Ryan L. Collins) · GitHub

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  1. HumanIdiogramLibrary HumanIdiogramLibrary Public

    Resource of human chromosome schematics & images

    96 12

  2. CNView CNView Public

    Visualization and annotation of CNVs from population-scale whole-genome sequencing data

    R 73 10

  3. RLCtools RLCtools Public

    R library of helper functions used across projects

    R

  4. broadinstitute/gatk-sv broadinstitute/gatk-sv Public

    A structural variation pipeline for short-read sequencing

    Python 206 82

  5. talkowski-lab/rCNV2 talkowski-lab/rCNV2 Public

    Aggregation and analyses of rare CNVs across diseases

    R 15 4

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