✂️ ⚡ Rapid haploid variant calling and core genome alignment
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Updated
Dec 12, 2025 - Perl
✂️ ⚡ Rapid haploid variant calling and core genome alignment
A haplotype analysis toolkit for natural variation study.
Simultaneous detection of SNPs and Indels using a 16-genotype probabilistic model
The SSRG pipeline was created as a simple and focused tool to investigate genetic diversity between genomes.
A pipeline to call SNPs, and SV from low coverage WGRS data
Bioinformatics analysis used to determine reinfection and relapse tuberculosis using whole genome sequencing data.
Pipeline which make phylogeny with sequence of different sample
A collection of scripts documenting the parameter settings used to apply variant discovery to the exploration of Duodenal Polyposis.
Archive of personal scripts repository from my various projects in the Buell Lab at MSU (Jan. 2008 - Apr. 2011)
Quickly identify and generate primers for diagnostic loci
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