GeneMANIA / genemaniaLinks
GeneMANIA helps you predict the function of your favourite genes and gene sets.
☆42Updated last year
Alternatives and similar repositories for genemania
Users that are interested in genemania are comparing it to the libraries listed below
Sorting:
- MyGene.info: A BioThings API for gene annotations☆127Updated last month
- 3D hotspot mutation proximity analysis tool☆47Updated 2 years ago
- Search across publicly available datasets to find instances where a drug or cell line of interest has been profiled.☆46Updated 6 years ago
- IPAW: a Nextflow workflow for proteogenomics☆28Updated 11 months ago
- Extension of the WGCNA program to improve the eigengene similarity of modules and increase the overall number of genes in modules.☆64Updated 4 years ago
- MuPeXI: the mutant peptide extractor and informer, a tool for predicting neo-epitopes from tumor sequencing data.☆51Updated 5 years ago
- ☆41Updated 7 years ago
- A quick and flexible single-cell RNA-seq processing framework on the cloud☆38Updated 5 years ago
- ARCHS4 RNA-seq processing scripts and web server pages.☆57Updated 4 years ago
- UC Santa Cruz Computational Genomics Lab's Toil-based RNA-seq pipeline☆41Updated 4 years ago
- Differential Count Data Analysis Toolbox☆61Updated last year
- ☆33Updated 4 years ago
- BAGEL software☆28Updated last year
- OLD REPOSITORY - Go to☆31Updated 7 years ago
- ☆35Updated 9 years ago
- integrated RNA-seq Analysis Pipeline☆84Updated 6 years ago
- PathwayMapper: An interactive and collaborative graphical curation tool for cancer pathways☆59Updated last year
- GTEx Visualizations☆64Updated 4 years ago
- Create a *de novo* alternative splicing database, validate splicing events, and quantify percent spliced-in (Psi) from RNA seq data☆66Updated 5 years ago
- This repository is the working directory for the Garnet-Forest bundle of python scripts for analyzing diverse forms of 'omic' data in a n…☆31Updated 6 years ago
- Accessing Intra-Tumor Heterogeneity and Tracking Longitudinal and Spatial Clonal Evolutionary History by Next-Generation Sequencing.☆69Updated 3 years ago
- Computational correction of copy-number effect in CRISPR-Cas9 essentiality screens☆29Updated 6 years ago
- Automated generation of tailored bioinformatics Jupyter Notebooks via a user interface.☆115Updated last month
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆84Updated last month
- Scalable RNA-seq analysis☆73Updated 4 years ago
- CICERO: a versatile method for detecting complex and diverse driver fusions using cancer RNA sequencing data.☆39Updated 2 months ago
- ChIP-seq DC and QC Pipeline☆34Updated 4 years ago
- Preprocessing of single-cell RNA-Seq (deprecated)☆62Updated 6 years ago
- Classifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests☆49Updated 11 months ago
- Rna-seq pipeline, From FASTQ to differential expression analysis...☆21Updated 8 years ago