A standalone and free application to explore genetics variations from VCF file

A utility to merge a large number of VCF files incrementally

Classes and functions for use with bioinformatics.

Your VCF converted to XLS from now. VCF stands for Variant Call Format and it is used by bioinformatics projects to encode structural genetic variants.

A Haskell script that performs basic parsing on the default output of ensembl-vep and variant-calling format (vcf) files.

High-throughput Tabular Data Processor (HTDP)

Variant Calling with Deep Learning for Prokaryotic genomes using TensorFlow. Adds (0 <= P(Variant) <= 1) to VCF files under INFO as abbreviated "ACC=".

SAMtools and BCFtools (v1.10) for manipulating next-generation sequencing data, from bioconda

Converts XLSX documents into VCF (Variant Call Format) - remastered for JDK1.8 2023

Convert an standard VCF to JSON format

A simple python implementation of Variant Call Format intersection and complements for identifying genetic mutations

A Haskell script for selecting variants from a variant calling format (vcf) file based on variants present in a mgibed file.

A WDL-based workflow for extraction of variants and their associated info from large VCF files

Convert genomic coordinates from the Human Genome version 19 (hg19) to version 38 (hg38)

Predicting true low-VAF SNVs in HPV using triplicate NGS samples and machine learning