XWangLabTHU / DISMIR
☆23Updated 3 years ago
Alternatives and similar repositories for DISMIR:
Users that are interested in DISMIR are comparing it to the libraries listed below
- Main repository for Drews et al. (Nature, 2022)☆39Updated last year
- This method uses shallow Whole Genome Sequencing (sWGS) and the segmentation of a genomic profile to assess the Homologous Recombination …☆34Updated 9 months ago
- ☆28Updated last year
- MutSig2CV from Lawrence et al. 2014☆31Updated 4 years ago
- A flexible framework for nucleosome profiling of cell-free DNA☆27Updated last year
- Package for calculation of Homologous Recombination Deficiency☆13Updated 5 years ago
- Clonality Inference in Multiple Tumor Samples using Phylogeny☆14Updated 9 years ago
- CNApp represents the first web tool to perform a comprehensive and integrative analysis of copy number alterations (CNAs) in a user-frien…☆20Updated 5 years ago
- ☆25Updated last year
- Fork of the Polysolver project☆31Updated 5 years ago
- All-FIT - Allele-Frequency-based Imputation of Tumor Purity☆17Updated 5 years ago
- A pipeline for identifying indel derived neoantigens using RNA-Seq data☆30Updated 2 years ago
- single-nucleus nanopore reads processing pipeline☆15Updated last year
- Code accompanying Characterizing genetic intra-tumor heterogeneity across 2,658 human cancer genomes☆43Updated 4 years ago
- High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants☆22Updated 5 years ago
- CLIP-seq Analysis of Multi-mapped reads☆30Updated 3 years ago
- ☆34Updated 2 years ago
- documentation for trackViewer☆29Updated 5 years ago
- Integrative analysis pipeline for pooled CRISPR functional genetic screens☆30Updated last year
- ☆15Updated last year
- Methods and analysis for Garcia-Nieto, et al. Somatic mutations☆15Updated 5 years ago
- direct comparison of circular and linear RNA expression☆22Updated 4 years ago
- ☆19Updated 7 years ago
- Process m6A/MeRIP-seq data in a single or batch job mode☆20Updated 4 years ago
- A statistical tool to detect differential alternative splicing events using single-cell RNA-seq☆22Updated last year
- ☆38Updated 5 years ago
- Genomic Identification of Significant Targets in Cancer (GISTIC), version 2☆51Updated 3 years ago
- ☆17Updated 3 years ago
- A neoantigen calling pipeline begins from variants record file (MAF) (Not maintain now)☆29Updated 5 years ago
- MAnorm2 for Normalizing and Comparing ChIP-seq Samples☆32Updated 2 years ago