{% extends "base_template.html" %} {% load static %} {% load humanize %} {% block title %}OMA Orthology database{% endblock %} {% block meta_description %}OMA is a method and database for the inference of orthologs among complete genomes. We provide browsable orthology predictions, APIs, flat file downloads and a standalone version of the inference algorithm.{% endblock %} {% block meta_hook %} {% endblock %} {% block js_hook %}{{ block.super }} {% if use_schema_dot_org %} {% endif %} {% endblock js_hook %} {% block content %}
Expand (e.g. to paste a long amino-acid sequence)
Examples: {% block search_examples %} Entry DROVI00099 - Entry Sting - Search for "immunity" - "obscura" species {% endblock search_examples %}
Introduction to OMA: See OMA in a nutshell (Introduction) in OMA doc.
Familiarise yourself with orthology basics: Swiss Orthology , Orthology benchmark.
Familiarise yourself with the different types of homologs in the OMA doc.
Get ideas about different types of analyses you could do with OMA.
If you use OMA in your work, please consider citing:
Altenhoff A et al., OMA orthology in 2021: website overhaul, conserved isoforms, ancestral gene order and more
Nucleic Acids Research, gka1007,
(doi:10.1093/nar/gkaa1007)