gerstung-lab / MutationTimeR
An R package to time somatic mutations
☆61Updated 4 years ago
Alternatives and similar repositories for MutationTimeR:
Users that are interested in MutationTimeR are comparing it to the libraries listed below
- An R package for studying mutational signatures and structural variant signatures along clonal evolution in cancer.☆71Updated 11 months ago
- Genomic Identification of Significant Targets in Cancer (GISTIC), version 2☆51Updated 3 years ago
- Public repository containing research code for the TCGA PanCanAtlas Splicing project☆41Updated 4 years ago
- Create mutation signatures from MAF's, and decompose them into Stratton signatures☆60Updated 5 years ago
- An R package for predicting HR deficiency from mutation contexts☆28Updated 2 months ago
- This method uses shallow Whole Genome Sequencing (sWGS) and the segmentation of a genomic profile to assess the Homologous Recombination …☆34Updated 9 months ago
- A modular, containerized pipeline for ATAC-seq data processing☆57Updated last month
- ☆38Updated 5 years ago
- MutSig2CV from Lawrence et al. 2014☆31Updated 4 years ago
- Dirichlet Process based methods for subclonal reconstruction of tumours☆29Updated last month
- ☆47Updated 3 months ago
- Code accompanying Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes☆43Updated 4 years ago
- Rocking R at UMCCR☆9Updated 4 years ago
- Battenberg R package for subclonal copynumber estimation☆86Updated last month
- R package containing useful functions for mutational signature analysis☆81Updated last week
- Filtering of PDX samples for mouse derived reads☆27Updated 2 years ago
- DCC/DAC methylation pipeline source☆55Updated 4 years ago
- Explore, compare, and evaluate Bioconductor packages related to genomic copy number analysis☆21Updated 2 years ago
- ROSE: RANK ORDERING OF SUPER-ENHANCERS☆47Updated 9 months ago
- DeCiFer is an algorithm that simultaneously selects mutation multiplicities and clusters SNVs by their corresponding descendant cell frac…☆20Updated 11 months ago
- Reference transcriptome indices build from kallisto for popular organisms☆42Updated last year
- Main repository for Drews et al. (Nature, 2022)☆39Updated last year
- mutation(barcode) caller for 10x single cell data☆44Updated 4 years ago
- Analysis of subclonal copy number alterations (CNA) and loss of heterozygosity (LOH) in cancer☆97Updated 4 years ago
- RepEnrich2 is an updated method to estimate repetitive element enrichment using high-throughput sequencing data.☆39Updated 3 years ago
- Mutational signature analysis for low statistics SNV data☆63Updated 8 months ago
- Tutorial Website☆59Updated 4 years ago
- Automate Absolute Copy Number Calling using 'ABSOLUTE' package☆40Updated last year
- QDNAseq package for Bioconductor☆50Updated 9 months ago
- ☆13Updated 7 years ago