XWangLabTHU / DISMIRLinks
☆25Updated 4 years ago
Alternatives and similar repositories for DISMIR
Users that are interested in DISMIR are comparing it to the libraries listed below
Sorting:
- ☆31Updated last year
- Clonality Inference in Multiple Tumor Samples using Phylogeny☆15Updated 10 years ago
- A flexible framework for nucleosome profiling of cell-free DNA☆29Updated 2 years ago
- This method uses shallow Whole Genome Sequencing (sWGS) and the segmentation of a genomic profile to assess the Homologous Recombination …☆36Updated 4 months ago
- Main repository for Drews et al. (Nature, 2022)☆42Updated 2 years ago
- MeRIPseqPipe:An integrated analysis pipeline for MeRIP-seq data based on Nextflow.☆42Updated last year
- ☆38Updated 5 years ago
- Clinical interpretation of somatic mutations in cancer☆50Updated 11 months ago
- MutSig2CV from Lawrence et al. 2014☆33Updated 5 years ago
- MAnorm2 for Normalizing and Comparing ChIP-seq Samples☆32Updated 3 years ago
- An R package to time somatic mutations☆65Updated 5 years ago
- ☆19Updated 7 years ago
- Homologous recombination deficiency in TCGA PanCancer Atlas☆29Updated 5 years ago
- ☆44Updated 7 years ago
- Identifying genome-wide translated open reading frames using ribosome profiling☆24Updated 2 years ago
- direct comparison of circular and linear RNA expression☆23Updated 5 years ago
- ☆27Updated 2 years ago
- All-FIT - Allele-Frequency-based Imputation of Tumor Purity☆18Updated 6 years ago
- ☆76Updated 4 years ago
- A detailed guide to analise and integrate small-RNASeq and RNASeq samples using miARma-Seq☆11Updated 6 years ago
- a versatile and flexible pipeline for analysing different variants of ChIA-PET data☆36Updated last year
- EasyFuse is a pipeline for accurate fusion gene detection from RNA-seq data.☆64Updated 2 weeks ago
- ☆36Updated 3 years ago
- ☆49Updated 3 years ago
- Automate Absolute Copy Number Calling using 'ABSOLUTE' package☆41Updated 2 years ago
- ☆23Updated 3 years ago
- CLIP-seq Analysis of Multi-mapped reads☆31Updated 4 years ago
- RNA editing tests☆17Updated 5 years ago
- RADAR is devised to detect and visualize all possible twelve-types of RNA editing events from RNA-seq datasets.☆20Updated 5 months ago
- Fork from https://bitbucket.org/mcgranahanlab/lohhla/src, modified for MSKCC needs☆32Updated 2 years ago