tkzeng / GeneBayesLinks
☆28Updated 4 months ago
Alternatives and similar repositories for GeneBayes
Users that are interested in GeneBayes are comparing it to the libraries listed below
Sorting:
- Immuological gene typing and annotation for genome assembly☆38Updated 7 months ago
- 🤖 Open‑source deep-learning-based splice‑site predictor that decodes splicing patterns across species☆28Updated 3 months ago
- ☆20Updated last year
- ☆23Updated 10 months ago
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆44Updated last week
- Analysis of gene expression and splicing diversity in a subset of samples from the 1000 Genomes Project, including eQTL and sQTL discover…☆42Updated last year
- Automated Detection and Qualification of Differential Methylation☆14Updated last year
- ☆29Updated 3 months ago
- A segmentation approach to analyze DNA methylation patterns and identify differentially methylation regions from whole-genome datasets☆19Updated last week
- Tools for merging Tandem Repeat VCF files☆36Updated 6 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 6 months ago
- A pipeline creation tool using Snakemake☆11Updated last week
- Runs a combination of tools to generate structural variant calls on short-read whole-genome sequencing data☆22Updated 3 years ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated 2 weeks ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- End-guided RNA assembler☆15Updated 2 months ago
- Repository for pipeline code☆26Updated last year
- Easy genomic regions for short-read variant calling☆44Updated last month
- A command line tool to compute mapping statistics from a BAM file☆25Updated 3 years ago
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆41Updated last month
- Functions to compare a SV call sets against a truth set.☆30Updated 4 months ago
- Package Homepage: http://bioconductor.org/packages/devel/bioc/html/DRIMSeq.html Bug Reports: https://support.bioconductor.org/p/new/post/…☆11Updated 5 years ago
- ☆20Updated 3 years ago
- ☆34Updated 10 months ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 3 years ago
- Sashimi plots for RNA-seq data using detected transcripts☆29Updated 7 months ago
- Two pass alignment for long reads☆22Updated 4 years ago
- Code and Tutorials for Running the MArginal ePIstasis Test (MAPIT)☆15Updated 2 years ago
- LongcallR is a SNP caller for single molecule long-read RNA-seq data☆67Updated last month
- Flexible linear mixed model framework for Genome Wide Association Studies☆18Updated 3 weeks ago