Collecting Genotypes from ENA and make their SNPs
-
Updated
Sep 27, 2021 - Python
#
snp-calling
Here are 3 public repositories matching this topic...
A Python bioinformatics tool for genomic pseudo-alignment, variant calling (SNPs), and coverage analysis.
-
Updated
Jan 3, 2026 - Python
This repository contains a Python script that queries NCBI to retrieve detailed information about SNPs (Single Nucleotide Polymorphisms) and parses the returned data. The script makes a request to the NCBI API, parses the XML data, and organizes the information into tables using pandas.
-
Updated
Apr 13, 2025 - Python
Improve this page
Add a description, image, and links to the snp-calling topic page so that developers can more easily learn about it.
Add this topic to your repo
To associate your repository with the snp-calling topic, visit your repo's landing page and select "manage topics."