vcf
Here are 149 public repositories matching this topic...
Personalized Genomics and Proteomics. Main diet: Ensembl, side dishes: SNPs
-
Updated
Oct 12, 2023 - Python
Structural variant toolkit for VCFs
-
Updated
May 10, 2024 - Python
Convert SNPs in VCF format to PHYLIP, NEXUS, binary NEXUS, or FASTA alignments for phylogenetic analysis
-
Updated
Jul 7, 2023 - Python
Bayesian genotyper for structural variants
-
Updated
Mar 6, 2021 - Python
tools for reading, writing, merging, and remapping SNPs
-
Updated
May 8, 2024 - Python
Python 3 library with good support for both reading and writing VCF
-
Updated
Mar 20, 2024 - Python
Python API for comprehensive GWAS analysis using GEMMA
-
Updated
Sep 6, 2023 - Python
🔧 Simple script in python to convert CSV files to VCF
-
Updated
Mar 22, 2024 - Python
vembrane filters VCF records using python expressions
-
Updated
Mar 26, 2024 - Python
Generic human DNA variant annotation pipeline
-
Updated
Feb 13, 2024 - Python
A python parser to simplify and build the VCF (Variant Call Format).
-
Updated
Dec 15, 2020 - Python
Genomic VCF to tab-separated values
-
Updated
Mar 9, 2023 - Python
VarFish: comprehensive DNA variant analysis for diagnostics and research
-
Updated
May 10, 2024 - Python
Convert GWAS summary statistics to VCF
-
Updated
Mar 11, 2023 - Python
Improve this page
Add a description, image, and links to the vcf topic page so that developers can more easily learn about it.
Add this topic to your repo
To associate your repository with the vcf topic, visit your repo's landing page and select "manage topics."