tkzeng / GeneBayesLinks
☆29Updated 5 months ago
Alternatives and similar repositories for GeneBayes
Users that are interested in GeneBayes are comparing it to the libraries listed below
Sorting:
- 🤖 Open‑source deep-learning-based splice‑site predictor that decodes splicing patterns across species☆30Updated 4 months ago
- Tools for merging Tandem Repeat VCF files☆37Updated 6 months ago
- Automated Detection and Qualification of Differential Methylation☆14Updated 2 years ago
- Immuological gene typing and annotation for genome assembly☆38Updated 8 months ago
- ☆30Updated 4 months ago
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Updated last year
- ☆23Updated 11 months ago
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆44Updated last month
- A segmentation approach to analyze DNA methylation patterns and identify differentially methylation regions from whole-genome datasets☆19Updated 3 weeks ago
- Evolutionary Transcriptomics with R☆49Updated last week
- Rapid and accurate ancestry inference using SNVs.☆28Updated 3 months ago
- End-guided RNA assembler☆15Updated 2 weeks ago
- fastest GTF/GFF-to-BED converter chilling around☆28Updated last month
- tspex: tissue-specificity calculator☆34Updated 2 years ago
- A command line tool to compute mapping statistics from a BAM file☆25Updated 3 years ago
- ☆20Updated last year
- Abismal is a mapper of FASTQ bisulfite-converted short reads (between 50 and 1000 bases) to a FASTA reference genome.☆19Updated last month
- interactive plots for differential expression analysis☆34Updated 5 months ago
- A comprehensive toolkit for mutational signature analysis☆42Updated last year
- Alternative polyadenylation detection from diverse data sources such as 3'-seq, long-read and short-reads.☆31Updated 2 years ago
- Scoring GT/AG sites for improving spliced alignment☆46Updated last week
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 9 months ago
- Splice junction analysis and filtering from BAM files☆42Updated 3 years ago
- Easy genomic regions for short-read variant calling☆45Updated 2 months ago
- FREE Divergence Error-Correcting DNA Barcodes☆10Updated 7 years ago
- Flexible linear mixed model framework for Genome Wide Association Studies☆18Updated 2 weeks ago
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆57Updated 8 months ago
- Sweep Inference Framework (controlling for correlation)☆29Updated last year
- ☆34Updated last week
- ☆37Updated last year