Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
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Updated
Jul 7, 2023 - Python
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
C-Phasing/CPhasing: Phasing and scaffolding polyploid genomes based on 3C-based data (Pore-C, CiFi, Hi-C, Omni-C).
Using de-novo assembly and read-phasing to assemble reference-free diploid genomes
Short Sequence Rastreator allows genetic diversity analysis and preparation of input files for other softwares such as STRUCTURE, DARwin and SPAGeDi.
LCVCFtools is a program designed for working with VCF files generated from low-coverage whole genome sequencing
Simulator for the Wright-Fisher model of genetic drift for haploid and diploid populations
This is a modified version of C-Phasing -- zgtools
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