Welcome to OpenOmics's documentation!

This Python package provide a series of tools to integrate and query the genomics, transcriptomics, proteomics, and
clinical data (aka, the multi-omics data). With scalable data-frame manipulation tools, OpenOmics facilitates the common
coding tasks when preparing data for RNA-seq bioinformatics analysis.

Features

• Provides a bioinformatics workflow to generate integrative results from multi-omics data.
• Facilitates integration of various bio-databases, multi-omics expression, genomics, and clinical data.
• Highly flexible to different data types and missing data.
• Provides researchers with means to consistently store and explore their experimental datasets.
• Enables scalable performance with parallel computing, while easily configurable to deploy on both single machine and a
  cluster.

Table of Content

:maxdepth: 2
:caption: Using OpenOmics Python API
:name: mastertoc
installation
usage/getting-started
usage/import-your-dataset
usage/annotate-external-databases
usage/network-data
usage/preprocess-downstream-analysis

:maxdepth: 1
:caption: API Reference

modules/openomics.multiomics
modules/openomics.annotate
modules/openomics.database.annotation
modules/openomics.database.sequence
modules/openomics.database.interaction
modules/openomics.database.disease
modules/openomics.database.ontology
modules/openomics.utils

:maxdepth: 1
:caption: MISC

misc/faq

:maxdepth: 1
:caption: Contributing and releases

contributing
history