✂️ ⚡ 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
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
R haploid sperm/oocyte data imputation (rhapsodi). A package for analysis of low-coverage single-cell sequencing data from multiple gametes.
Simulator for the Wright-Fisher model of genetic drift for haploid and diploid populations
Available at: https://clstacy.github.io/yeastKODoublingTimes/ . Doubling time estimates for haploid KO library, data from doi: 10.1093/g3journal/jkac240
Analysis scripts for "A method for low-coverage single-gamete sequence analysis demonstrates adherence to Mendel's first law across a large sample of human sperm" https://elifesciences.org/articles/76383
Wrigh Fisherman Simulation for Haploid population
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