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MiModD

Analyzed 2 days ago

MiModD is an integrated solution for mapping-by-sequencing analysis of whole-genome sequencing (WGS) data from laboratory model organisms. It enables geneticists to identify the genetic mutations present in an organism starting from just raw WGS read data and a reference genome without the help of a ... [More]

16.8K lines of code

0 current contributors

almost 4 years since last commit

0 users on Open Hub

Inactive

I Use This

Mostly written in Python

Tags bioinformatics galaxy genome mapping_by_sequencing model_organisms mutation_identification read_alignment sequencing variant_calling

GEMINI Genome Mining

G

Analyzed 2 days ago

A lightweight DB framework for disease and population genetics.

27.6K lines of code

3 current contributors

almost 5 years since last commit

0 users on Open Hub

Inactive

I Use This

Mostly written in Python

Tags bioinformatics python variant_calling vcf

VCF4J

V

Analyzed 2 days ago

Java utils for parsing the variant call format

1.72K lines of code

0 current contributors

over 3 years since last commit

0 users on Open Hub

Inactive

I Use This

Mostly written in Java

Licenses: apache_2

Tags bioinformatics call exome format genome lifescience sequencing variant variant_calling vcf