jonahcullen / wagsLinks
☆18Updated last week
Alternatives and similar repositories for wags
Users that are interested in wags are comparing it to the libraries listed below
Sorting:
- Population-wide Deletion Calling☆35Updated 3 months ago
- What is true, thank you, ernestly. A large variant benchmarking tool analogous to hap.py for small variants.☆32Updated last year
- PopSTR - A Population based microsatellite genotyper☆33Updated last year
- Immuological gene typing and annotation for genome assembly☆37Updated 4 months ago
- Alignment-free genotyper for SNPs and short indels, implemented in Python.☆49Updated 4 months ago
- SAMStat displays various properties of next-generation sequencing reads stored in SAM/BAM format.☆24Updated last year
- Exact Tandem Repeat Finder (not a TRF replacement)☆49Updated 5 years ago
- Structural variant (SV) analysis tools☆36Updated last year
- ☆31Updated 2 years ago
- A tutorial on structural variant calling for short read sequencing data☆39Updated 8 months ago
- SV analysis of the long-read sequencing data of the 1019 samples of the 1KG-ONT panel☆25Updated 2 months ago
- ☆16Updated 6 months ago
- An insertion caller for Illumina paired-end WGS data.☆23Updated 11 months ago
- Improved structural variant discovery in accurate long reads using sample-specific strings (SFS)☆43Updated last month
- Structural variant VCF annotation, duplicate removal and comparison☆33Updated 4 months ago
- Pipeline to evaluate and validate the accuracy of variant calling methods in genomic research☆31Updated last week
- for visual evaluation of read support for structural variation☆54Updated last year
- Fast sequencing data quality metrics☆26Updated last month
- Structural variant merging tool☆52Updated 10 months ago
- Location of public benchmarking; primarily final results☆18Updated 5 months ago
- Efficient and accurate pathogenicity prediction for coding and regulatory structural variants in long-read genome sequencing☆36Updated last year
- MethPhaser: methylation-based haplotype phasing of human genomes☆48Updated 4 months ago
- This tools counts the number of specific k-mers within sequence data. The counts can then be compare to other counts to determine to comp…☆29Updated 7 months ago
- Pipeline for structural variant image curation and analysis.☆48Updated 3 years ago
- Master of Pores 2☆23Updated 7 months ago
- ☆35Updated 4 years ago
- lossless nanopore pod5 <=> s/blow5 file conversion☆40Updated last week
- ☆30Updated 2 years ago
- WDL workflows for variant calling and assembly using ONT☆35Updated last month
- MarginPolish: Graph based assembly polishing☆46Updated 4 years ago