A python library to develop genomic data simulators
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Updated
Aug 29, 2023 - Python
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.
echoverse module: Single- and multi-threaded downloading functions.
Put a face and name to the number that texts you 6 digits when you try to login.
A command-line parser for VCF files designed for population genetics analyses.
SAMtools and BCFtools (v1.10) for manipulating next-generation sequencing data, from bioconda
Variant annotation and filtration server ALAPY Genome Explorer
Simple tool to merge VCF contacts.
Pipeline to analyze structural variants producing VCF files, then merge them and annotate if in Exon.
htslib for the zig build system
to analyze multiple VCF files and generate a summary of variant metrics
Example files for Benin NGS capacity building project
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.
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