zhejilab / RibORFLinks
Identifying genome-wide translated open reading frames using ribosome profiling
☆23Updated 2 years ago
Alternatives and similar repositories for RibORF
Users that are interested in RibORF 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…☆26Updated last year
- A list of alternative splicing analysis resources☆46Updated 7 months ago
- direct comparison of circular and linear RNA expression☆22Updated 4 years ago
- CLIP-seq Analysis of Multi-mapped reads☆31Updated 4 years ago
- EasyFuse is a pipeline for accurate fusion gene detection from RNA-seq data.☆62Updated 2 weeks ago
- ☆23Updated 4 years ago
- RNA editing quantification in deep transcriptome data☆15Updated 3 months ago
- ☆15Updated 3 years ago
- Workflows for processing RNA data for germline short variant discovery with GATK v4 and related tools☆80Updated 4 years ago
- RADAR is devised to detect and visualize all possible twelve-types of RNA editing events from RNA-seq datasets.☆20Updated last month
- A tool for accurately detecting actively translating ORFs from Ribo-seq data☆39Updated 8 months ago
- Bioinformatic tool for Splice site Strength Estimation using RNA-seq☆19Updated 3 months ago
- A Python3-base pipeline for translated circular RNA(circRNA) identification☆18Updated 3 weeks ago
- A statistical tool to detect differential alternative splicing events using single-cell RNA-seq☆22Updated 2 years ago
- optimization of ribosome P-site positioning in ribosome profiling data☆55Updated 8 months ago
- An R package to process and analyze transcriptomic data☆18Updated 4 months ago
- Process m6A/MeRIP-seq data in a single or batch job mode☆20Updated 5 years ago
- Estimation of Promoter Activity from RNA-Seq data☆56Updated 3 months ago
- RNA editing tests☆17Updated 5 years ago
- Estimate locus specific human LINE-1 expression.☆39Updated last month
- A Perl/R pipeline for plotting metagenes☆37Updated 4 years ago
- Tutorial Website☆61Updated 4 years ago
- Full-length transcriptome splicing and mutation analysis☆84Updated last year
- Demultiplexes a fastq.☆47Updated 4 years ago
- An Integrated Analysis Pipeline for Unbiased ChIP seq Analysis☆22Updated last year
- Single cell Nanopore sequencing data for Genotype and Phenotype☆54Updated 5 months ago
- Benchmarking long-read RNA-seq analysis tools☆27Updated 8 months ago
- REDItools are python scripts to investigate RNA editing at genomic scale.☆68Updated 3 months ago
- SpecHLA reconstructs entire diploid sequences of HLA genes and infers LOH events. It supports HLA-A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, …☆51Updated 2 weeks ago
- polyApipe☆19Updated 8 months ago