tkzeng / GeneBayes
☆25Updated 11 months ago
Alternatives and similar repositories for GeneBayes:
Users that are interested in GeneBayes are comparing it to the libraries listed below
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆24Updated 6 months ago
- ☆21Updated 3 months ago
- Snakemake workflow for Illumina RNA-sequencing experiments - extract population genomic signals from RNA-Seq data☆18Updated 3 months ago
- ☆26Updated last year
- Flexible linear mixed model framework for Genome Wide Association Studies☆19Updated last month
- ☆30Updated 10 months ago
- ☆28Updated 3 months ago
- Analysis of gene expression and splicing diversity in a subset of samples from the 1000 Genomes Project, including eQTL and sQTL discover…☆36Updated 8 months ago
- Code and Tutorials for Running the MArginal ePIstasis Test (MAPIT)☆14Updated 2 years ago
- ☆17Updated 2 years ago
- SpliceWiz is an R package for exploring differential alternative splicing events in splice-aware alignment BAM files.☆17Updated 3 weeks ago
- ☆27Updated last year
- Liftover VCF files☆17Updated 8 years ago
- Evolutionary Transcriptomics with R☆42Updated 3 weeks ago
- Immuological gene typing and annotation for genome assembly☆35Updated 2 weeks ago
- ☆20Updated last year
- BiSulfite Bolt - A Bisulfite Sequencing Alignment and Processing Tool☆21Updated 2 years ago
- CADD-SV – a framework to score the effect of structural variants☆14Updated 2 weeks ago
- Sweep Inference Framework (controlling for correlation)☆29Updated 8 months ago
- FINSURF is a tool designed to analyse lists of sequences variants in the human genome.☆12Updated 2 years ago
- A command line tool to compute mapping statistics from a BAM file☆23Updated 3 years ago
- interactive plots for differential expression analysis☆32Updated last week
- Copy Number Methods for Detection and Genome Wide Association Tests☆22Updated 4 months ago
- SQUID detects both fusion-gene and non-fusion-gene structural variations from RNA-seq data☆42Updated 2 years ago
- ERVcaller is a tool designed to accurately detect and genotype non-reference unfixed endogenous retroviruses (ERVs) and other transposabl…☆13Updated last year
- Automated Detection and Qualification of Differential Methylation☆12Updated last year
- Useful tools for working with Salmon output☆37Updated 4 years ago
- A pipeline creation tool using Snakemake☆11Updated last week
- a lexicographically-based GTF/GFF sorter☆32Updated 7 months ago
- DNA multiple sequence aligner, official version from Penn State's Miller Lab☆31Updated 6 years ago