A python library to develop genomic data simulators

Collection of several small tools. These tools stay here temporarily and may move to other major repositories as they evolve.

It reads all values ​​in certain rows and columns in Excel and converts phone number values ​​to vcf. It can be converted to vcf by typing the prefix we want to add to the required section in the code. Adds phone numbers to our contact list in seconds. It has a simple and useful interface.

Various scripts for working with NGS data in file formats such as VCF, BAM/SAM, and JSON

Processing text files and converting them into a VCF file form which contacts can be imported to the mobile phone

A Python GUI program with VCF file manipulation features like Creating, exporting.

The main aim of this little project is to compare the European allele frequencies of the 1k genomes project with the gnomad frequencies.

A python parser for vcf bioinformatics file

Identifies structural variant (SV) sites shared between two VCF files.

to analyze multiple VCF files and generate a summary of variant metrics

A utility to merge a large number of VCF files incrementally

Export the phone numbers from your Excel file to a VCF file using Python.

Lightweight standalone tool to reduce size of VCF files through filtering

The repository processes a VCF file to filter and transform its data based on specific genomic criteria.

Vannatator

A script that takes user input to create a .vcf file and a QR-Code that contains this file.

Python Script for converting .csv contact files to .vcf.

A quick way to visualize VCF data in a html report