snugel / cas-offinderLinks
An ultrafast and versatile algorithm that searches for potential off-target sites of CRISPR/Cas-derived RNA-guided endonucleases.
☆94Updated 3 years ago
Alternatives and similar repositories for cas-offinder
Users that are interested in cas-offinder are comparing it to the libraries listed below
Sorting:
- Analysis pipeline for the GUIDE-seq assay.☆80Updated 2 years ago
- All source code of the crispor.org website☆79Updated 2 weeks ago
- Fast and flexible ORF finder☆75Updated 3 years ago
- Analysis pipeline for the GUIDE-seq assay.☆27Updated last month
- Public repository for ShapeMapper 2 releases☆39Updated 9 months ago
- Capturing protein-RNA interaction footprints from single-nucleotide CLIP-seq data☆32Updated 4 years ago
- Neoantigens prediction pipeline for multi- or single-region vcf files using ANNOVAR and netMHCpan.☆111Updated last year
- FlashFry: The rapid CRISPR target site characterization tool☆78Updated last year
- Tool package to perform in-silico CRISPR analysis and assessment☆31Updated last year
- Sequana: a set of Snakemake NGS pipelines☆146Updated last month
- trackplot is a tool for visualizing various next-generation sequencing (NGS) data, including DNA-seq, RNA-seq, single-cell RNA-seq and fu…☆97Updated this week
- CADD scripts release for offline scoring. For more information about CADD, please visit our website☆85Updated 3 months ago
- A workflow for enhanced protein isoform detection through integration of long-read RNA-seq and mass spectrometry-based proteomics.☆48Updated 2 years ago
- HTSeq is a Python library to facilitate processing and analysis of data from high-throughput sequencing (HTS) experiments.☆106Updated 3 months ago
- Pair-End AssembeR☆32Updated 11 years ago
- Helper scripts for biological data processing from Sentieon☆64Updated 3 weeks ago
- Code for the CRISPOR article, all data and code to create figures and analysis☆44Updated 9 years ago
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆42Updated 3 weeks ago
- A small-RNA sequencing analysis pipeline☆92Updated 3 months ago
- Discovering known and novel miRNAs from small RNA sequencing data☆154Updated last year
- deep residual neural network for classifying the pathogenicity of missense mutations.☆115Updated 4 years ago
- Pangolin is a deep-learning method for predicting splice site strengths.☆78Updated last year
- Pure-python implementation of UCSC liftOver genome coordinate conversion☆97Updated last year
- Contains the code from "Learning the Sequence Determinants of Alternative Splicing from Millions of Random Sequences"☆35Updated 9 years ago
- Tools for manipulating biological data, particularly multiple sequence alignments☆158Updated this week
- ☆57Updated 5 years ago
- Variant calling tool for long-read sequencing data☆111Updated 6 months ago
- Fast HLA type inference from whole-genome data☆137Updated 5 months ago
- On-Target and Off-Target Scoring Algorithms for CRISPR gRNAs☆20Updated 2 months ago
- A set of Shiny apps to provide interactive enrichment analysis and exploration of results.☆31Updated this week