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☆31Updated 2 weeks ago
- Immuological gene typing and annotation for genome assembly☆38Updated 8 months ago
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆44Updated this week
- ☆24Updated 11 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 8 months ago
- ☆30Updated 5 months ago
- interactive plots for differential expression analysis☆34Updated 5 months ago
- Isoform-level functional RNA-Seq analysis 🧬☆35Updated last month
- A command line tool to compute mapping statistics from a BAM file☆25Updated 3 years ago
- Rapid and accurate ancestry inference using SNVs.☆28Updated 3 months ago
- Evolutionary Transcriptomics with R☆49Updated 3 weeks ago
- FREE Divergence Error-Correcting DNA Barcodes☆10Updated 7 years ago
- Tools for merging Tandem Repeat VCF files☆37Updated 7 months ago
- LongcallR is a SNP caller for single molecule long-read RNA-seq data☆69Updated this week
- ☆20Updated 3 years ago
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Updated last year
- ☆21Updated last year
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆57Updated 9 months ago
- Package Homepage: http://bioconductor.org/packages/devel/bioc/html/DRIMSeq.html Bug Reports: https://support.bioconductor.org/p/new/post/…☆12Updated 5 years ago
- End-guided RNA assembler☆15Updated last week
- R API for browsing, analyzing, and manipulating reference-aligned genome graphs in a GenomicRanges framework☆41Updated this week
- ☆20Updated 2 years ago
- Alternative polyadenylation detection from diverse data sources such as 3'-seq, long-read and short-reads.☆31Updated 2 years ago
- Two pass alignment for long reads☆22Updated 4 years ago
- tspex: tissue-specificity calculator☆35Updated 2 years ago
- A set of tools to annotate VCF files with expression and readcount data☆29Updated 9 months ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 9 months ago
- Structural variant VCF annotation, duplicate removal and comparison☆34Updated last month
- R package for DNA methylation analysis☆19Updated last year
- Method for performing genome-wide association like studies on neighborhoods identified on biological networks relevant for the phenotype …☆16Updated 2 years ago