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@WGLab

Wang Genomics Lab

We develop software tools for genome analysis

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  1. doc-ANNOVAR doc-ANNOVAR Public

    Documentation for the ANNOVAR software

    234 359

  2. InterVar InterVar Public

    A bioinformatics software tool for clinical interpretation of genetic variants by the 2015 ACMG-AMP guideline

    Python 188 92

  3. dragonstar2019 dragonstar2019 Public

    135 98

  4. DeepMod DeepMod Public

    DeepMod: a deep-learning tool for genomic-scale, strand-sensitive and single-nucleotide based detection of DNA modifications

    Python 101 35

  5. NanoCaller NanoCaller Public

    Variant calling tool for long-read sequencing data

    Python 101 8

  6. PennCNV PennCNV Public

    Copy number vaiation detection from SNP arrays

    C 89 55

Repositories

Showing 10 of 81 repositories
  • ContextSV Public

    An alignment-based, generalized structural variant caller for long-read sequencing/mapping data

    WGLab/ContextSV’s past year of commit activity
    C++ 2 MIT 0 5 0 Updated Nov 15, 2024
  • NanoCaller Public

    Variant calling tool for long-read sequencing data

    WGLab/NanoCaller’s past year of commit activity
    Python 101 MIT 8 29 0 Updated Nov 15, 2024
  • PhenoGPT Public
    WGLab/PhenoGPT’s past year of commit activity
    Jupyter Notebook 19 MIT 5 3 0 Updated Nov 11, 2024
  • PhenoGPT2 Public

    PhenoGPT2 is an advanced phenotype recognition model, leveraging the robust capabilities of large language models.

    WGLab/PhenoGPT2’s past year of commit activity
    Python 1 MIT 0 0 0 Updated Oct 30, 2024
  • doc-ANNOVAR Public

    Documentation for the ANNOVAR software

    WGLab/doc-ANNOVAR’s past year of commit activity
    234 359 123 0 Updated Oct 24, 2024
  • InFuse Public

    InFuse: Isoform Novety and Fusion Detection

    WGLab/InFuse’s past year of commit activity
    Python 0 0 0 0 Updated Oct 24, 2024
  • SCOTCH Public

    Single-Cell Omics for Transcriptome CHaracterization (SCOTCH): isoform-level characterization of gene expression through long-read single-cell RNA sequencing

    WGLab/SCOTCH’s past year of commit activity
    Python 5 MIT 0 2 0 Updated Oct 22, 2024
  • LongReadSum Public
    WGLab/LongReadSum’s past year of commit activity
    C++ 13 MIT 2 5 0 Updated Sep 27, 2024
  • phenopacket2prompt Public Forked from monarch-initiative/phenopacket2prompt

    GA4GH Phenopacket to LLM prompt

    WGLab/phenopacket2prompt’s past year of commit activity
    Java 0 MIT 1 0 0 Updated Sep 15, 2024
  • Gene-Fusion-Detection-Pipeline-LRS Public

    The Gene Fusion (GF) Detection Pipeline is comprehensive bioinformatics workflow designed for Oxford Nanopore long-read sequencing data.

    WGLab/Gene-Fusion-Detection-Pipeline-LRS’s past year of commit activity
    Python 1 0 0 0 Updated Aug 30, 2024
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