YangLab / RADARLinks
RADAR is devised to detect and visualize all possible twelve-types of RNA editing events from RNA-seq datasets.
☆20Updated 2 weeks ago
Alternatives and similar repositories for RADAR
Users that are interested in RADAR are comparing it to the libraries listed below
Sorting:
- single-cell-Isoform-Sequencing-Analysis-Tools: New and powerful tools brings single-cell RNA sequencing to the Isoform level and single m…☆25Updated last year
- ☆25Updated last year
- Identifying genome-wide translated open reading frames using ribosome profiling☆23Updated 2 years ago
- A statistical tool to detect differential alternative splicing events using single-cell RNA-seq☆22Updated 2 years ago
- A R script to perform clustering of gene expression time-series RNA-seq data with Mfuzz.☆22Updated 6 years ago
- ☆51Updated last year
- RNA editing tests☆17Updated 4 years ago
- MAnorm2 for Normalizing and Comparing ChIP-seq Samples☆32Updated 2 years ago
- Benchmarking long-read RNA-seq analysis tools☆27Updated 7 months ago
- MeRIPseqPipe：An integrated analysis pipeline for MeRIP-seq data based on Nextflow.☆41Updated last year
- CLIP-seq Analysis of Multi-mapped reads☆31Updated 4 years ago
- Main repository for Drews et al. (Nature, 2022)☆42Updated 2 years ago
- An Integrated Analysis Pipeline for Unbiased ChIP seq Analysis☆22Updated 11 months ago
- ☆23Updated 4 years ago
- polyApipe☆18Updated 7 months ago
- Analysis pipeline for our circSC manuscript☆14Updated 3 years ago
- EasyFuse is a pipeline for accurate fusion gene detection from RNA-seq data.☆61Updated 9 months ago
- A list of alternative splicing analysis resources☆46Updated 5 months 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
- ☆15Updated 3 years ago
- Uncertainty-aware quantification of Transposable Elements expression in scRNA-seq☆19Updated this week
- Model-based analysis of APA using 3' end-linked reads☆10Updated 4 years ago
- A pipeline for identifying indel derived neoantigens using RNA-Seq data☆30Updated 3 years ago
- The Spatial Splicing-derived Neoantigen Identifier Pipeline (SSNIP) allows for the precise characterization of neoantigens derived from c…☆20Updated 5 months ago
- A script to make downloading of SRA/GEO data easier☆31Updated last year
- scripts for the integrating ATAC-seq, RNA-seq and CHi-C paper☆24Updated 2 years ago
- ☆20Updated 5 years ago
- Code repo for all analysis done for the 'Pan-cancer whole genome comparison of primary and metastatic solid tumors' study.☆18Updated 2 years ago
- software for analysis of chromatin feature occupancy profiles from high-throughput sequencing data☆17Updated 5 years ago
- Data of genome annotation from full-stack ChromHMM model trained with 1032 datasets from 127 reference epigenomes☆37Updated last year