rikenbit / ramdaqLinks
☆13Updated 3 months ago
Alternatives and similar repositories for ramdaq
Users that are interested in ramdaq are comparing it to the libraries listed below
Sorting:
- Tool package to perform in-silico CRISPR analysis and assessment☆27Updated last year
- FRACTAL: framework for distributed computing to trace large accurate lineages☆24Updated 2 years ago
- Ultra-efficient and sensitive method to search for Open Reading Frames in spliced genomes guided by reference annotation to maximize prot…☆28Updated 3 weeks ago
- RIblast is ultrafast RNA-RNA interaction prediction software based on seed-and-extension algorithm for comprehensive lncRNA interactome a…☆17Updated 2 years ago
- ☆14Updated 2 years ago
- PhyloCSF++ computes PhyloCSF tracks for whole-genome multiple sequence alignments, scores single MSA, annotates CDS features in GFF/GTF f…☆31Updated 3 years ago
- POC Nextflow pipeline to run the Chai-1, SOTA model for biomolecular structure prediction☆11Updated 4 months ago
- Python bindings for the TaxonKit library☆40Updated 3 weeks ago
- A genome browser in your Jupyter notebook☆31Updated 3 weeks ago
- The RepeatScout 1.0.5, written by Pevzner et al., source code for browsing. The official release and more information are available at h…☆15Updated 2 years ago
- Ultra rapid nanopore whole genome sequencing pipeline, published in https://www.nature.com/articles/s41587-022-01221-5☆20Updated 11 months ago
- Master of Pores 2☆23Updated 6 months ago
- Read, parse and operate different multiple input file formats with OpenVariant☆12Updated last week
- Ultra-fast 5' and 3' demultiplexer☆27Updated last year
- Generation and update of protein families☆14Updated 2 weeks ago
- An insertion caller for Illumina paired-end WGS data.☆23Updated 10 months ago
- DeepSig - Predictor of signal peptides in proteins based on deep learning☆26Updated 2 years ago
- A Python module to analyze Sanger sequencing results.☆24Updated last year
- 🧬 MSABrowser: dynamic and fast visualization of sequence alignments, variations, and annotations☆32Updated last year
- BigSeqKit: a parallel Big Data toolkit to process FASTA and FASTQ files at scale☆55Updated last year
- Metagenome analysis using the Kraken software suite☆32Updated 2 years ago
- A tool for simulating random mutations in any genome☆38Updated last year
- Toolkit for the design and analysis of amplicon sequencing experiments utilizing unique molecular identifiers (UMIs)☆41Updated last year
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- Convert genbank files to a swath of other formats☆18Updated last year
- Metagenomic search for novel CRISPR-transposons☆12Updated 3 years ago
- Quality assessment of de novo transcriptome assemblies from RNA-Seq data☆22Updated 7 months ago
- Improved Inference of Ortholog Groups using Hidden Markov Models☆34Updated 3 months ago
- Parse GFF3 into Pandas dataframes☆27Updated last year
- visual analysis of your VCF files☆33Updated 2 years ago