MathOnco / EvoFreqLinks
Evolutionary frequency visualization tool of temporal data
☆23Updated 3 years ago
Alternatives and similar repositories for EvoFreq
Users that are interested in EvoFreq are comparing it to the libraries listed below
Sorting:
- Interactive R package to quantify, analyse and visualise alternative splicing☆37Updated this week
- A small R package to make sequencing read coverage plots in R.☆39Updated 3 years ago
- The official repository of the Bioconductor 2019 Conference Workshops☆25Updated 2 years ago
- An R Bioconductor package providing interactive connections to igv.js (the Integrative Genomics Viewer) in a web browser☆46Updated 9 months ago
- An R for fast and flexible DNA methylation analysis☆33Updated last month
- iread☆25Updated 4 years ago
- A tidy interface for coverage analysis☆30Updated 5 years ago
- satuRn is a highly performant and scalable method for performing differential transcript usage analyses.☆22Updated 2 years ago
- knowledge-based genotyping of cancer hotspots from the tumor BAM files☆21Updated 3 years ago
- Differential expression and allelic analysis, nonparametric statistics☆29Updated 7 months ago
- Create a cromphensive report of DEG list coming from any analysis of RNAseq data☆25Updated last year
- An R package to interpret biological trends from DNA methylation data☆18Updated 3 years ago
- CNAqc - Copy Number Alteration (CNA) Quality Check package☆22Updated 3 months ago
- Filter and prioritize fusion calls☆20Updated 10 months ago
- RNA-seq quantifications: gene expression responses to human rhinovirus infection for 6 asthmatic and 6 non-asthmatic donors (SRP046226)☆19Updated 7 years ago
- RNA-seq for Mendelian disease diagnostics: A hands-on tutorial through bioinformatic tools and workflows☆17Updated 3 years ago
- R package providing Variance Stabilizing Transformations appropriate for RNA-Seq data☆21Updated 3 months ago
- Toolkit for QTL mapping and meta-analysis.☆17Updated 3 years ago
- A Package For Predicting The Disruptiveness Of Single Nucleotide Polymorphisms On Transcription Factor Binding Sites.☆29Updated last year
- Pipeline for the identification of cancer-related mutations from RNA-seq data☆14Updated 4 years ago
- Molecular Signatures Database (MSigDB) in a data frame☆16Updated 6 years ago
- Co-expression network management based on WGCNA + k-means☆19Updated 4 years ago
- Code for creating cell-type-specific regulatory element annotation files☆18Updated last year
- ☆10Updated 6 years ago
- An R Package for Geneset Enrichment Workflows☆76Updated 2 weeks ago
- Visualise correlation results and test significancies of these☆23Updated 5 years ago
- 📊 An R package of RNA-seq workflow☆16Updated 3 years ago
- Flexible Bayesian inference of mutational signatures☆36Updated 2 years ago
- Transcript quantification import with automatic metadata detection☆68Updated this week
- Python function for TMB snake plots☆16Updated 5 years ago