# vcf-kit

**Repository Path**: scnet-lib/VCF-kit

## Basic Information

- **Project Name**: vcf-kit
- **Description**: No description available
- **Primary Language**: Unknown
- **License**: MIT
- **Default Branch**: master
- **Homepage**: None
- **GVP Project**: No

## Statistics

- **Stars**: 0
- **Forks**: 0
- **Created**: 2023-10-24
- **Last Updated**: 2024-01-05

## Categories & Tags

**Categories**: Uncategorized

**Tags**: None

## README

[![Build Status](https://travis-ci.org/AndersenLab/VCF-kit.svg?branch=master)](https://travis-ci.org/AndersenLab/VCF-kit) [![Coverage Status](https://coveralls.io/repos/github/AndersenLab/vcf-kit/badge.svg?branch=master)](https://coveralls.io/github/AndersenLab/vcf-kit?branch=master) [![Documentation Status](https://readthedocs.org/projects/vcf-kit/badge/?version=latest)](http://vcf-kit.readthedocs.io/en/latest/?badge=latest)


VCF-kit - [Documentation](http://vcf-kit.readthedocs.io/en/latest/?badge=latest)
===========

VCF-kit is a command-line based collection of utilities for performing analysis on Variant Call Format (VCF) files. A summary of the commands is provided below.

| Command |Description                                                                                 |
|:----------|------------------------------------------------------------------------------------------|
| __calc__ | Obtain  frequency/count of  genotypes and alleles.                                               |
| __call__ | Compare variants  identified  from  sequences obtained  through alternative methods against a VCF. |
| __filter__ | Filter  variants  with  a minimum or  maximum number  of  REF,  HET,  ALT,  or  missing calls.         |
| __geno__ | Various operations  at  the genotype  level.                                                      |
| __genome__ | Reference genome  processing  and management.                                                  |
| __hmm__ | Hidden-markov model for use in  imputing  genotypes from  parental  genotypes in  linkage studies.   |
| __phylo__ | Generate  dendrograms from  a VCF.                                                              |
| __primer__ | Generate  primers for variant validation.                                                     |
| __rename__ | Add a prefix, suffix, or  substitute  a string  in  sample  names.                                |
| __tajima__ | Calculate Tajima’s  D.                                                                        |
| __vcf2tsv__ | Convert a VCF to  TSV.                                                                       |

## Installation

__VCF-Kit has been upgraded to Python 3__

VCF-kit has been tested with Python 3.6. VCF-kit makes use of additional software for a variety of tasks:

* bwa (v 0.7.12)
* samtools (v 1.3)
* bcftools (v 1.3)
* blast (v 2.2.31+)
* muscle (v 3.8.31)
* primer3 (v 2.5.0)

You can install these dependencies and VCF-kit using conda, or you can use a Docker image.

#### Conda

```bash
conda config --add channels bioconda
conda config --add channels conda-forge
conda create -n vcf-kit \
  danielecook::vcf-kit=0.2.6 \
  "bwa>=0.7.17" \
  "samtools>=1.10" \
  "bcftools>=1.10" \
  "blast>=2.2.31" \
  "muscle>=3.8.31" \
  "primer3>=2.5.0"

conda activate vcf-kit
```

#### Docker

You can also run VCF-kit with all installed dependencies using docker: 

```bash
docker run -it andersenlab/vcf-kit vk
```