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    • fusion transcript detection using long reads, leveraging ctat-minimap2 and FusionInspector
      Perl
      123100Updated Oct 4, 2025Oct 4, 2025
    • Python
      51731Updated Aug 11, 2025Aug 11, 2025
    • benchmarking utilities for ctat-mutations
      Python
      0100Updated Jul 30, 2025Jul 30, 2025
    • A versatile pairwise aligner for genomic and spliced nucleotide sequences
      C
      448100Updated Jul 1, 2025Jul 1, 2025
    • Software used by Trinity CTAT for building CTAT Genome Libs, resource databases shared by Trinity CTAT components
      Perl
      310113Updated Apr 28, 2025Apr 28, 2025
    • detection of cancer splicing aberrations
      Perl
      2990Updated Apr 4, 2025Apr 4, 2025
    • rnaseqc

      Public
      Fast, efficient RNA-Seq metrics for quality control and process optimization
      C++
      20000Updated Nov 26, 2024Nov 26, 2024
    • Mutation detection using GATK4 best practices and latest RNA editing filters resources. Works with both Hg38 and Hg19
      HTML
      1877440Updated Jul 20, 2024Jul 20, 2024
    • Python
      0000Updated Jun 24, 2024Jun 24, 2024
    • 3312031Updated Sep 5, 2023Sep 5, 2023
    • WDL
      1100Updated Jul 7, 2023Jul 7, 2023
    • BatVI

      Public
      WDL and docker image for running BatVI
      WDL
      1000Updated Dec 22, 2022Dec 22, 2022
    • A copy of VirusFinder2/VERSE, used for identifying viral integrations.
      C
      3000Updated Apr 6, 2022Apr 6, 2022
    • ViFi

      Public
      Pipeline for identifying viral integration and fusion mRNA reads from NGS data. Manuscript is currently in preparation.
      Python
      17000Updated Mar 18, 2022Mar 18, 2022
    • 0200Updated Mar 7, 2022Mar 7, 2022
    • extended testing data for ctat mutations pipe
      0100Updated Aug 26, 2021Aug 26, 2021
    • arcasHLA

      Public
      Fast and accurate in silico inference of HLA genotypes from RNA-seq
      Python
      59000Updated Apr 14, 2021Apr 14, 2021
    • code for running alternative rna-based variant detection tools and benchmarking
      Python
      2000Updated May 18, 2020May 18, 2020
    • tools for adding mutations to existing .bam files, used for testing mutation callers
      Python
      86000Updated Jun 14, 2019Jun 14, 2019
    • find viruses and microbes using centrifuge
      Perl
      0000Updated Apr 19, 2019Apr 19, 2019
    • mutations

      Public
      calling variants from RNA-Seq data
      Python
      1400Updated Nov 10, 2017Nov 10, 2017
    • Genome guided transcript reconstruction
      0000Updated Oct 24, 2017Oct 24, 2017
    • transcript expression quantification
      0000Updated Oct 24, 2017Oct 24, 2017
    • lncRNA

      Public
      lncRNA classification
      0000Updated Oct 24, 2017Oct 24, 2017