ActiveDriverDB
☆12May 1, 2023Updated 2 years ago
Alternatives and similar repositories for ActiveDriverDB
Users that are interested in ActiveDriverDB are comparing it to the libraries listed below. We may earn a commission when you buy through links labeled 'Ad' on this page.
Sorting:
- Multi-omics disease sub-type specific drug repositioning aided with expression signatures from ConnectivityMap☆19Mar 7, 2020Updated 6 years ago
- R package for metabolic enzyme enrichment anaylsis☆13Oct 24, 2025Updated 5 months ago
- "Independent Component Analysis of BIg Omics Data"☆13Nov 3, 2022Updated 3 years ago
- Sequence to Medical Phenotypes: A pipeline featuring variant annotation, prioritization, pharmacogenomics, and tools for analyzing genomi…☆13Mar 1, 2016Updated 10 years ago
- NaRnEA (Nonparametric analytical Rank-based Enrichment Analysis)☆11Mar 2, 2023Updated 3 years ago
- ☆15Dec 9, 2019Updated 6 years ago
- Classifies genes as an oncogene, tumor suppressor gene, or as a non-driver gene by using Random Forests☆50Aug 3, 2024Updated last year
- Structural Variant Prediction Viewer☆35Jul 19, 2017Updated 8 years ago
- Regulatory networks with Direct Information☆17Oct 14, 2019Updated 6 years ago
- ☆17May 5, 2020Updated 5 years ago
- Learn tissue-specificity and tissue-sharing of genetic regulation across 49 tissues using constraint matrix factorization model☆22Oct 9, 2020Updated 5 years ago
- OUTRIDER: OUTlier in RNA-seq fInDER is an R-based framework to find aberrantly expressed genes in RNA-seq data☆56Feb 11, 2026Updated last month
- Subsampling of high-throughput sequencing count data☆20May 10, 2019Updated 6 years ago
- NGS perl modules☆11Updated this week
- reverse gene expression score☆15Sep 8, 2023Updated 2 years ago
- Jax code for functional genomics ML☆14Mar 5, 2025Updated last year
- Publication Page for ArchR Manuscript 2020☆23Aug 17, 2021Updated 4 years ago
- Bioconductor components for general cancer genomics☆11Feb 5, 2023Updated 3 years ago
- Add functional variant annotation to MAF file☆11Nov 20, 2024Updated last year
- A server for maintaining high-throughput sequencing QC data☆13Aug 5, 2025Updated 7 months ago
- ☆12Jul 5, 2024Updated last year
- Repository to perform mapping of new datasets to the Human Lung Cell Atlas.☆20Jun 7, 2023Updated 2 years ago
- Supplementary files for paper "Detection and removal of barcode swapping in single-cell RNAseq".☆11Jul 5, 2018Updated 7 years ago
- Bioinformatics tools for dealing with Multiple Alignment Format (MAF) files.☆11Jul 8, 2025Updated 8 months ago
- A collection of CSV/TSV Utilities☆13Jun 2, 2020Updated 5 years ago
- Repository of "Personalization of Logical Models With Multi-Omics Data Allows Clinical Stratification of Patients" paper☆11Dec 2, 2025Updated 3 months ago
- ☆11Feb 6, 2023Updated 3 years ago
- The project for analyzing differential methylation of MeRIP-seq data☆24Sep 5, 2023Updated 2 years ago
- BANDITS: Bayesian ANalysis of DIfferenTial Splicing☆19Sep 29, 2025Updated 5 months ago
- Supervised Adversarial Alignment of Single-Cell RNA-seq Data☆32Feb 6, 2020Updated 6 years ago
- predicts neoepitopes from phased somatic mutations detected using tumor/normal DNA-seq data☆27Sep 13, 2023Updated 2 years ago
- ☆13Nov 30, 2018Updated 7 years ago
- rbioapi: User-Friendly R Interface to Biologic Web Services' API☆24Jan 26, 2026Updated last month
- Implementation of the cellular Potts model in pure javascript for fun an easy visualisation.☆11Mar 7, 2019Updated 7 years ago
- SV clustering☆31Jul 5, 2021Updated 4 years ago
- ☆27Mar 2, 2026Updated 3 weeks ago
- Code available for the quantitative pharmacophores☆13Sep 7, 2022Updated 3 years ago
- Repository of the pipeline of computational methods for logical modelling of biological networks that are deregulated in diseases, develo…☆10Mar 14, 2026Updated last week
- Convert numpy mask to dicom rtstruct☆13Feb 28, 2023Updated 3 years ago