formbio / laavaLinks
LAAVA: Long-read AAV Analysis
☆13Updated last week
Alternatives and similar repositories for laava
Users that are interested in laava are comparing it to the libraries listed below
Sorting:
- Build an index for your BAM Index (BAI)☆17Updated 10 years ago
- Cromwell output organizer☆13Updated 4 years ago
- Customer workshop materials☆18Updated 2 years ago
- ☆16Updated 11 months ago
- Quality of life improvements for Bioinformatics in Python.☆31Updated this week
- Variant catalogue pipeline☆26Updated 7 months ago
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Rust UMI Directional Adjacency Deduplicator☆15Updated 6 years ago
- Freelance bioinformaticians directory☆10Updated 2 years ago
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Updated last year
- Location of public benchmarking; primarily final results☆18Updated 10 months ago
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- A better, faster way to count guides in CRISPR screens.☆34Updated 8 months ago
- ☆13Updated 3 years ago
- RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes☆18Updated 5 years ago
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- 🧬 MSABrowser: dynamic and fast visualization of sequence alignments, variations, and annotations☆35Updated last year
- ☆22Updated 2 years ago
- Intersect multiple VCF files with haplotype awareness☆25Updated 4 years ago
- 🍶 Genome assembly with short sequence reads☆25Updated last year
- add true-negative SVs from a population callset to a truth-set.☆15Updated 3 years ago
- A wrapper for calling small variants from human germline high-coverage single-sample Illumina data☆14Updated 6 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Updated 6 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 10 months ago
- overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites☆33Updated 6 months ago
- mreps: software for tandem repeat identification in DNA☆15Updated 6 years ago
- k-mer similarity analysis pipeline☆23Updated last month
- CLI to automate Nextflow pipeline testing☆12Updated this week
- Demonstrating best practices for bioinformatics command line tools☆26Updated 5 years ago
- Stupid Simple Structural Variant View☆25Updated 9 years ago