dzhakparov / GeneSelectRLinks
☆19Updated last year
Alternatives and similar repositories for GeneSelectR
Users that are interested in GeneSelectR are comparing it to the libraries listed below
Sorting:
- ☆17Updated last year
- ☆23Updated 3 years ago
- Pipeline to analyze long-read mRNA isoforms and ORF products sequenced in breast cancer using PacBio Single-Molecule technology.☆16Updated 3 years ago
- Analysis and visualization of RNA-Seq results☆29Updated 2 months ago
- The Spatial Splicing-derived Neoantigen Identifier Pipeline (SSNIP) allows for the precise characterization of neoantigens derived from c…☆18Updated 3 months ago
- Pseudotime Analysis for Bulk Data☆16Updated last year
- HTCA Analysis Tools☆6Updated 2 years ago
- GEfetch2R - Access Single-cell/Bulk RNA-seq Data from Public Repositories and Benchmark the Subsequent Format Conversion Tools☆36Updated 4 months ago
- ☆20Updated last year
- Code related to scRNA analysis using the scAmpi workflow☆27Updated last month
- Easy and comprehensive biological network reconstruction and analysis☆31Updated 10 months ago
- ☆9Updated last month
- QBRC Neoantigen calling pipeline with CSiN calculation embedded☆24Updated 3 years ago
- Immune Cell Gene Signatures for Profiling the Microenvironment of Solid Tumours☆27Updated 4 years ago
- Matrix factorization model for interpreting single cell gene expression in biologically heterogeneous data☆21Updated last year
- GENIE3 (GEne Network Inference with Ensemble of trees) R-package☆33Updated 3 years ago
- Epigenetic cell-type deconvolution from Single-Cell Omic Reference profiles☆33Updated 4 months ago
- Example of run CytoSig and reproduce prediction results on bulk and single-cell cohorts☆13Updated 2 years ago
- ☆22Updated last year
- ☆17Updated last year
- Analytical tools and pipelines for bulk and single cell epigenomic and human genetic data☆27Updated 4 years ago
- ☆28Updated last year
- A R script to perform clustering of gene expression time-series RNA-seq data with Mfuzz.☆22Updated 6 years ago
- This repository aims to serve as an index of the work described at Salmen & De Jonghe et. al 2022☆23Updated 3 years ago
- Combined mutation recurrence and functional impact to identify coding and non-coding cancer drivers☆15Updated 6 years ago
- Methods to use SNPs or gene expression to classify single cell RNAseq to reference profiles☆29Updated 5 years ago
- Methods and analysis for Garcia-Nieto, et al. Somatic mutations☆15Updated 5 years ago
- Tools for assessing clustering robustness☆25Updated last week
- Network construction Algorithm☆22Updated 11 months ago
- Collection of functions created and/or curated to aid in the visualization and analysis of single-cell data using R.☆16Updated 3 years ago