AlexandrovLab / SigProfilerMatrixGeneratorLinks
SigProfilerMatrixGenerator creates mutational matrices for all types of somatic mutations. It allows downsizing the generated mutations only to parts for the genome (e.g., exome or a custom BED file). The tool seamlessly integrates with other SigProfiler tools.
☆109Updated 3 weeks ago
Alternatives and similar repositories for SigProfilerMatrixGenerator
Users that are interested in SigProfilerMatrixGenerator are comparing it to the libraries listed below
Sorting:
- Assignment of known mutational signatures to individual samples and individual somatic mutations☆56Updated last week
- SigProfilerExtractor allows de novo extraction of mutational signatures from data generated in a matrix format. The tool identifies the n…☆160Updated 3 weeks ago
- ☆73Updated 2 months ago
- SigProfilerPlotting provides a standard tool for displaying all types of mutational signatures as well as all types of mutational pattern…☆48Updated 3 months ago
- Microsatellite instability (MSI) detection for tumor only data.☆106Updated last year
- ☆116Updated last year
- Somatic copy number analysis using WGS paired end wholegenome sequencing☆72Updated 4 years ago
- ☆117Updated last year
- ASCAT R package☆183Updated 3 months ago
- Battenberg R package for subclonal copynumber estimation☆88Updated 3 weeks ago
- Software program for checking sample matching for NGS data☆132Updated last year
- Analysis of subclonal copy number alterations (CNA) and loss of heterozygosity (LOH) in cancer☆97Updated 4 years ago
- deconstructSigs☆141Updated 2 years ago
- AmpliconArchitect (AA) is a tool to identify one or more connected genomic regions which have simultaneous copy number amplification and …☆147Updated last year
- HMMRATAC peak caller for ATAC-seq data☆100Updated 7 months ago
- STAR based ENCODE Long RNA-Seq processing pipeline☆94Updated 4 years ago
- R package containing useful functions for mutational signature analysis☆82Updated this week
- ☆92Updated this week
- An R package to time somatic mutations☆62Updated 4 years ago
- ☆69Updated last year
- Copy number calling and variant classification using targeted short read sequencing☆136Updated 2 months ago
- nextNEOpi: a comprehensive pipeline for computational neoantigen prediction☆73Updated 3 weeks ago
- A quickstart tool for AmpliconArchitect. Performs all preliminary steps (alignment, CNV calling, seed interval detection) required prior …☆67Updated 2 weeks ago
- SEACR: Sparse Enrichment Analysis for CUT&RUN☆110Updated 2 years ago
- This WDL pipeline implements data pre-processing and initial variant calling according to the GATK Best Practices for germline SNP and In…☆53Updated 4 years ago
- Inferring and visualizing clonal evolution in multi-sample cancer sequencing☆147Updated 4 years ago
- Check strandedness of RNA-Seq fastq files☆124Updated 2 years ago
- TPMCalculator quantifies mRNA abundance directly from the alignments by parsing BAM files☆130Updated last year
- CoMut is a Python library for visualizing genomic and phenotypic information via comutation plots☆94Updated 10 months ago
- Script to automatically create and run IGV snapshot batchscripts☆141Updated 2 years ago