formbio / laavaLinks
LAAVA: Long-read AAV Analysis
☆13Updated last month
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
- Quality of life improvements for Bioinformatics in Python.☆31Updated last month
- Rust UMI Directional Adjacency Deduplicator☆15Updated 5 years ago
- add true-negative SVs from a population callset to a truth-set.☆15Updated 3 years ago
- ☆16Updated 9 months ago
- Location of public benchmarking; primarily final results☆18Updated 8 months ago
- python (cython) wrapper for https://github.com/ryanlayer/giggle for fast interval searching of huge datasets.☆16Updated 7 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Updated 3 years ago
- Library for indexing VCF files for random access searches by rsID☆17Updated 3 months ago
- ☆13Updated 3 years ago
- mreps: software for tandem repeat identification in DNA☆15Updated 5 years ago
- A better, faster way to count guides in CRISPR screens.☆33Updated 6 months ago
- Clair3-Trio: variant calling in trio using Nanopore long-reads☆16Updated last year
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Updated last year
- ☆22Updated 2 years ago
- Customer workshop materials☆18Updated 2 years ago
- Freelance bioinformaticians directory☆10Updated 2 years ago
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- BED QC tool (in the making)☆16Updated 3 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆28Updated 8 months ago
- Library for visualising genomic features in Python.☆15Updated 8 years ago
- 🍶 Genome assembly with short sequence reads☆26Updated last year
- Variant catalogue pipeline☆26Updated 6 months ago
- overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites☆33Updated 5 months ago
- Tools for generating and decoding error-correcting DNA barcodes☆15Updated 3 years ago
- Automated Detection and Qualification of Differential Methylation☆14Updated last year
- 🧬 MSABrowser: dynamic and fast visualization of sequence alignments, variations, and annotations☆35Updated last year
- Single-pass probabilistic duplicate marking of alignments with a Bloom filter.☆23Updated 2 years ago