crisprVerse / crisprDesign
Comprehensive design of CRISPR gRNAs for nucleases and base editors
☆22Updated last week
Alternatives and similar repositories for crisprDesign:
Users that are interested in crisprDesign are comparing it to the libraries listed below
- Analysis pipeline for the GUIDE-seq assay.☆23Updated 2 weeks ago
- Tool package to perform in-silico CRISPR analysis and assessment☆22Updated 9 months ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated 9 months ago
- Collection of R packages that work in harmony for CRISPR gRNA design☆13Updated last year
- On-Target and Off-Target Scoring Algorithms for CRISPR gRNAs☆16Updated 4 months ago
- Haplotype, isoform and gene level expression analysis using multi-mapping RNA-seq reads☆68Updated 11 months ago
- off-targeting assessment of Cas9 gRNAs☆13Updated 3 years ago
- Bioinformatic pipeline for identifying dsDNA breaks by marker based incorporation, such as breaks induced by designer nucleases like Cas9…☆21Updated 2 months ago
- GFF3sort: A Perl Script to sort gff3 files and produce suitable results for tabix tools☆48Updated 4 years ago
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆27Updated last year
- Detection of Circular RNA and Fusions from RNA-Seq☆32Updated 6 years ago
- Analysis pipeline for the GUIDE-seq assay.☆77Updated last year
- Pair-End AssembeR☆30Updated 10 years ago
- visual analysis of your VCF files☆31Updated 2 years ago
- alternative splicing analysis pipeline☆18Updated 3 years ago
- BEAVR: A Browser-based tool for the Exploration And Visualization of RNAseq data☆25Updated 3 years ago
- optimization of ribosome P-site positioning in ribosome profiling data☆48Updated this week
- Identifying genome-wide translated open reading frames using ribosome profiling☆21Updated last year
- Digenome-toolkit ver2.☆16Updated 3 years ago
- ☆54Updated 3 years ago
- Tools for analyzing DNA methylation data☆36Updated last week
- EditR: an algorithm for simple and cost effective measurement of base editing by quantifying Sanger trace fluorescence☆32Updated last year
- NANOME pipeline (Nanopore long-read sequencing data consensus DNA methylation detection)☆30Updated 11 months ago
- Useful tools for working with Salmon output☆37Updated 4 years ago
- ✂️ Deep learning-based splice site predictor that improves spliced alignments☆46Updated last month
- Flexible and efficient parsing, interpreting and editing of sequencing reads☆42Updated last month
- iCodon customizes gene expression based on the codon composition☆14Updated last year
- A tool for the calculation of RNA-editing index for RNA seq data☆40Updated last year
- SpecHLA reconstructs entire diploid sequences of HLA genes and infers LOH events. It supports HLA-A, -B, -C, -DPA1, -DPB1, -DQA1, -DQB1, …☆41Updated this week
- A Perl/R pipeline for plotting metagenes☆37Updated 3 years ago