There are 0 repository under variant-call-format topic.
A standalone and free application to explore genetics variations from VCF file
A utility to merge a large number of VCF files incrementally
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)
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)
Converts XLSX documents into VCF (Variant Call Format) - remastered for JDK1.8 2023
A Haskell script for selecting variants from a variant calling format (vcf) file based on variants present in a mgibed file.
Predicting true low-VAF SNVs in HPV using triplicate NGS samples and machine learning
SAMtools and BCFtools (v1.10) for manipulating next-generation sequencing data, from bioconda
Variant Calling with Deep Learning for Prokaryotic genomes using TensorFlow. Adds (0 <= P(Variant) <= 1) to VCF files under INFO as abbreviated "ACC=".