yoyoong / mHapSuiteLinks
☆12Updated 8 months ago
Alternatives and similar repositories for mHapSuite
Users that are interested in mHapSuite are comparing it to the libraries listed below
Sorting:
- Main repository for Drews et al. (Nature, 2022)☆41Updated last year
- single-cell-Isoform-Sequencing-Analysis-Tools: New and powerful tools brings single-cell RNA sequencing to the Isoform level and single m…☆24Updated 10 months ago
- A tool kit for dissecting cancer evolution from multi-region derived tumor biopsies via somatic mutations☆36Updated 3 years ago
- ☆11Updated 2 years ago
- A statistical tool to detect differential alternative splicing events using single-cell RNA-seq☆22Updated last year
- Code and data from Koche et al. Extrachromosomal circular DNA drives oncogenic genome remodeling in neuroblastoma (2020)☆15Updated 4 years ago
- MAnorm2 for Normalizing and Comparing ChIP-seq Samples☆33Updated 2 years ago
- ☆10Updated 2 years ago
- allele specific DNA methylation haplotype region☆14Updated last year
- ☆17Updated 4 years ago
- ☆17Updated 6 years ago
- scripts for the integrating ATAC-seq, RNA-seq and CHi-C paper☆24Updated 2 years ago
- Process m6A/MeRIP-seq data in a single or batch job mode☆20Updated 5 years ago
- SpliceWiz is an R package for exploring differential alternative splicing events in splice-aware alignment BAM files.☆18Updated 2 months ago
- R package to calculate the Aneuploidy Score from Chromosome Arm-level SCNAs/Aneuploidies (CAAs) as outlined and expanded by Shukla et al.…☆16Updated 4 years ago
- single-nucleus nanopore reads processing pipeline☆15Updated last year
- HiC for copy Number variation and Translocation detection☆39Updated 3 years ago
- BISulfite-seq CUI Toolkit☆19Updated 3 weeks ago
- TEProf2 Pipeline used to find promoters and predict protein sequences from RNA-sequencing data☆23Updated 2 years ago
- Scripts used for the ACT paper☆12Updated 4 years ago
- Arabidopsis RNA_-seq downstream analysis shiny app☆30Updated 5 years ago
- GENome Organisation Visual Analytics☆15Updated 3 years ago
- Micro DNA identification☆23Updated 3 years ago
- Code repo for all analysis done for the 'Pan-cancer whole genome comparison of primary and metastatic solid tumors' study.☆15Updated 2 years ago
- CLIP-seq Analysis of Multi-mapped reads☆30Updated 3 years ago
- A Deep Learning-Based Model for Quantifying Transposable Elements in Single-Cell Sequencing Data☆27Updated last month
- Analysis pipeline for our circSC manuscript☆13Updated 3 years ago
- ☆25Updated last year
- High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants☆22Updated 5 years ago
- Perform differential transcript usage (DTU) analysis of bulk or single-cell RNA-seq data. See documentation at:☆20Updated last year