formbio / laavaLinks
LAAVA: Long-read AAV Analysis
☆13Updated this week
Alternatives and similar repositories for laava
Users that are interested in laava are comparing it to the libraries listed below
Sorting:
- Cromwell output organizer☆13Updated 4 years ago
- Location of public benchmarking; primarily final results☆18Updated 5 months ago
- Samwell: a python package for using genomic files... well☆20Updated 3 years ago
- Build an index for your BAM Index (BAI)☆17Updated 10 years ago
- A phase-aware pharmacogenomic diplotyper for PacBio datasets☆16Updated last month
- An Artificial Neural Network-based discriminator for validating clinically significant genomic variants☆35Updated last year
- Structural Variation breakpoint discovery via adaptive learning☆15Updated 2 years ago
- prioritize effects of variant annotations from VEP, SnpEff, et al.☆34Updated 7 months ago
- robust matching of small variant datasets using flexible scoring schemes☆11Updated 5 years ago
- Simplify snpEff annotations for interesting cases☆22Updated 6 years ago
- A Computational Workflow for Designing Libraries of sgRNAs for CRISPR-Mediated Base Editing, and much more☆19Updated last year
- pathoscore evaluates variant pathogenicity tools and scores.☆21Updated 3 years ago
- Variant catalogue pipeline☆25Updated 2 months ago
- ☆16Updated 6 months ago
- ☆22Updated last year
- k-mer similarity analysis pipeline☆21Updated last week
- Simplifies parallel processing of DNA sequencing reads☆9Updated 9 months ago
- Tools for generating and decoding error-correcting DNA barcodes☆16Updated 3 years ago
- POSTRE: Prediction Of STRuctural variant Effects☆27Updated 4 months ago
- Library for indexing VCF files for random access searches by rsID☆17Updated last year
- filtering trio-based genetic variants in VCFs for clinical review☆21Updated 4 years ago
- RCK: Reconstruction of clone- and haplotype-specific Cancer Karyotypes☆17Updated 5 years ago
- CLI to automate Nextflow pipeline testing☆12Updated 2 weeks ago
- A wrapper for calling small variants from human germline high-coverage single-sample Illumina data☆14Updated 5 years ago
- Clair3-Trio: variant calling in trio using Nanopore long-reads☆15Updated last year
- A series of tools and pipelines for genotyping MHC / HLA genes and alleles using SMRT Sequencing☆21Updated 8 years ago
- Differential Mutation Analysis☆11Updated 5 years ago
- Customer workshop materials☆18Updated 2 years ago
- Fast, accurate and simple to use command line tool for variant detection in NGS data.☆12Updated 5 years ago
- ☆12Updated last year