An extendable parser for vcf files written in C++
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Updated
Apr 21, 2017 - C++
An extendable parser for vcf files written in C++
The main aim of this little project is to compare the European allele frequencies of the 1k genomes project with the gnomad frequencies.
Variant annotation and filtration server ALAPY Genome Explorer
Example files for Benin NGS capacity building project
Put a face and name to the number that texts you 6 digits when you try to login.
High-throughput Tabular Data Processor (HTDP)
Marketing + Contactual Entities (For Uploading CSV to maintain and allow people to control their information)
Python Script for converting .csv contact files to .vcf.
Collection of several small tools. These tools stay here temporarily and may move to other major repositories as they evolve.
Tools For Computational Biology
SAMtools and BCFtools (v1.10) for manipulating next-generation sequencing data, from bioconda
Integration of a MongoDB database for storing and filtering variant caller (VCF) file information
Simple tool to merge VCF contacts.
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