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    • fusion transcript detection using long reads, leveraging ctat-minimap2 and FusionInspector
      Perl
      Other
      01330Updated Oct 11, 2024Oct 11, 2024
    • detection of cancer splicing aberrations
      Perl
      Other
      2850Updated Sep 3, 2024Sep 3, 2024
    • Mutation detection using GATK4 best practices and latest RNA editing filters resources. Works with both Hg38 and Hg19
      HTML
      Other
      1873440Updated Jul 20, 2024Jul 20, 2024
    • Python
      0000Updated Jun 24, 2024Jun 24, 2024
    • benchmarking utilities for ctat-mutations
      Python
      0100Updated Jun 3, 2024Jun 3, 2024
    • Python
      BSD 3-Clause "New" or "Revised" License
      51331Updated Nov 22, 2023Nov 22, 2023
    • Software used by Trinity CTAT for building CTAT Genome Libs, resource databases shared by Trinity CTAT components
      Perl
      BSD 3-Clause "New" or "Revised" License
      210101Updated Oct 27, 2023Oct 27, 2023
    • 3411531Updated Sep 5, 2023Sep 5, 2023
    • A versatile pairwise aligner for genomic and spliced nucleotide sequences
      C
      Other
      409100Updated Aug 19, 2023Aug 19, 2023
    • rnaseqc

      Public
      Fast, efficient RNA-Seq metrics for quality control and process optimization
      C++
      Other
      19000Updated Aug 4, 2023Aug 4, 2023
    • WDL
      1100Updated Jul 7, 2023Jul 7, 2023
    • BatVI

      Public
      WDL and docker image for running BatVI
      WDL
      MIT License
      1000Updated Dec 22, 2022Dec 22, 2022
    • A copy of VirusFinder2/VERSE, used for identifying viral integrations.
      C
      MIT License
      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
      GNU General Public License v3.0
      18000Updated 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
      GNU General Public License v3.0
      50000Updated 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
      MIT License
      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