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
- Rust UMI Directional Adjacency Deduplicator☆15Updated 5 years ago
- Location of public benchmarking; primarily final results☆18Updated 6 months ago
- ☆16Updated 7 months ago
- Customer workshop materials☆18Updated 2 years ago
- 🍶 Genome assembly with short sequence reads☆25Updated last year
- POSTRE: Prediction Of STRuctural variant Effects☆27Updated 6 months ago
- Intersect multiple VCF files with haplotype awareness☆25Updated 4 years ago
- pathoscore evaluates variant pathogenicity tools and scores.☆22Updated 3 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Updated 5 years ago
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- Variant catalogue pipeline☆25Updated 4 months ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- overlapping bases in read-pairs from a fragment indicate accuracy and reveal error-prone sites☆33Updated 2 months ago
- RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes☆17Updated 5 years ago
- Listing of GPU based bioinformatics software & sites & publications☆10Updated 3 years ago
- BED QC tool (in the making)☆16Updated 3 years ago
- Fast sequencing data quality metrics☆27Updated 3 months ago
- A Python package for fast operations on 1-dimensional genomic signal tracks☆24Updated 5 years ago
- 🧬 High-performance VCF file parser and reformatter with VEP annotation support. Converts complex VCF files to analyzable TSV format …☆36Updated 2 weeks ago
- A wrapper for calling small variants from human germline high-coverage single-sample Illumina data☆14Updated 6 years ago
- ☆22Updated last year
- Rapid and accurate ancestry inference using SNVs.☆20Updated 2 weeks ago
- programs and scripts, mainly python, for analyses related to nucleic or protein sequences☆24Updated 3 weeks ago
- ☆12Updated last year
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Quality of life improvements for Bioinformatics in Python.☆30Updated this week
- Multithreaded read analysis☆19Updated last month