rraadd88 / beditor
A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more
☆17Updated 5 months ago
Related projects ⓘ
Alternatives and complementary repositories for beditor
- Tool package to perform in-silico CRISPR analysis and assessment☆22Updated 6 months ago
- Ultra-fast 5' and 3' demultiplexer☆24Updated 6 months ago
- GOMCL: a toolkit to cluster, evaluate, and extract non-redundant associations of Gene Ontology-based functions☆20Updated last year
- Identifying differentially methylated regions from MethylC-seq (bisulfite-sequencing) data☆26Updated last year
- BAGEL software☆26Updated 9 months ago
- Processing and plotting tools for genomics data☆20Updated this week
- Long read to rMATS☆31Updated last year
- ☆14Updated 2 years ago
- Versatile FASTA/FASTQ demultiplexer.☆32Updated 5 months ago
- A script to make downloading of SRA/GEO data easier☆30Updated last year
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated 6 months ago
- Comparison of Adaptive Immune Receptor Repertoires☆25Updated last year
- alternative splicing analysis pipeline☆17Updated 3 years ago
- Tools for generating and decoding error-correcting DNA barcodes☆16Updated 2 years ago
- ☆33Updated last month
- MetaLogo: a heterogeneity-aware sequence logo generator and aligner☆20Updated last year
- isoCirc☆10Updated 11 months ago
- ☆19Updated last month
- Annotation and segmentation of MAS-seq data☆20Updated last year
- Allo: a multi-mapped read rescue strategy for gene regulatory analyses☆23Updated 2 months ago
- A Nextflow pipeline to align, merge, and organize large PhIP-Seq datasets☆11Updated this week
- A p-value-free method for controlling false discovery rates in high-throughput biological data with two conditions☆38Updated 2 years ago
- Demonstrating best practices for bioinformatics command line tools☆26Updated 4 years ago
- Useful tools for working with Salmon output☆35Updated 4 years ago
- R package to analyze aberrant splicing junctions in tumor samples to identify neoepitopes☆13Updated this week
- The Isoforms from Single-Cell; Long-read Expression Suite☆18Updated 2 months ago
- Identifying genome-wide translated open reading frames using ribosome profiling☆20Updated last year
- A Python module to analyze Sanger sequencing results.☆18Updated 11 months ago
- ☆16Updated 5 years ago
- TIMEOR: Trajectory Inference and Mechanism Exploration with Omics Data in R☆17Updated 2 years ago