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Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
Created
2017-10-10
102 commits to master branch, last one about a year ago
Learning the Variant Call Format
Created
2015-06-05
172 commits to main branch, last one 6 months ago
GCP Variant Transforms
Created
2017-11-08
431 commits to master branch, last one 2 years ago
Rare variant test software for next generation sequencing data
Created
2013-01-09
1,204 commits to master branch, last one 3 years ago
Program for estimating πN/πS, dN/dS, and other diversity measures from next-generation sequencing data
Created
2015-05-24
236 commits to master branch, last one about a year ago
Rapid standardisation and quality control of GWAS or QTL summary statistics
Created
2021-03-30
402 commits to master branch, last one 10 days ago
Powerful statistics for VCF files
Created
2019-10-20
50 commits to master branch, last one about a year ago
create a interactive coverage plot dashboard from bam files and add gb, vcf and bed tracks
Created
2023-10-05
51 commits to master branch, last one about a month ago