Deepak Unni

Profile

12 years of experience developing and maintaining tools that support biological and biomedical research. I currently work as a Scientific Coordinator at the Swiss Personalized Health Network at SIB Swiss Institute of Bioinformatics, with a keen interest in biological data modeling, knowledge representation, open-source software development, ETL pipelines, ontology-driven data integration, and knowledge graphs. I am particularly interested in making datasets and other digital assets FAIR by leveraging rich metadata to improve their discovery, interoperability, and reuse across research communities.

Technical Skills

Languages

Python, Java

Semantic Web Standards

RDF(S), OWL, SPARQL, SHACL, ShEx, ODRL

Vocabularies

Dublin Core, DCAT, DCAT-AP, HealthDCAT-AP, VoID, PROV-O, SKOS

Ontologies

GO, HP, Mondo, OMO, SULO

Modeling frameworks

LinkML

Data Models

Biolink Model, InterMine, SPHN RDF Schema

Graph Databases

GraphDB, QLever, Apache Jena Fuseki, Neo4j

Health Data Standards

SNOMED CT, LOINC, ICD-10-GM, HL7 FHIR

Backend Frameworks

FastAPI, Flask

Experience

Aug 2022 – Present

Basel, Switzerland

Scientific Coordinator

SIB Swiss Institute of Bioinformatics
Swiss Personalized Health Network

SPHN is a national initiative led by the Swiss Academy of Medical Sciences and the SIB Swiss Institute of Bioinformatics. Broadly speaking, SPHN develops, implements, and validates coordinated data infrastructures that make health-related data available, interoperable, and shareable for research in Switzerland. As a Scientific Coordinator at the SPHN Data Coordination Center, I focus on the semantic and metadata foundations of these FAIR data infrastructures, where my work includes:

  • ·Engaging with clinical, research, and data provider stakeholders to capture domain semantics and formalize them in RDF
  • ·Leading the adoption of semantic web technologies for data modeling, knowledge representation, and validation of health-related data
  • ·Contributing to the design and evolution of the SPHN RDF Schema, integrating standard terminologies and ontologies to ensure semantic interoperability across Swiss hospitals
  • ·Supporting the development and maintenance of open-source tools and ETL pipelines that help data providers produce, validate, and deliver FAIR-compliant data
  • ·Building and deploying the SPHN Metadata Catalog, an end-to-end platform that makes SPHN data assets discoverable through rich, standards-based metadata
  • ·Interfacing with local and international initiatives to ensure that SPHN Metadata Catalog is interoperable with other FAIR data infrastructures and aligned with global standards
  • ·Promoting FAIR principles through documentation, training, and engagement with data providers, researchers and the broader scientific community

Apr 2021 – Jul 2022

Heidelberg, Germany

Software Developer

European Molecular Biology Laboratory
German Human Genome-Phenome Archive

The German Human Genome-Phenome Archive (GHGA) is a national initiative within Germany's National Research Data Infrastructure (NFDI) that provides a secure, FAIR-compliant platform for storing, sharing, and analyzing human omics data. In this role, I:

  • ·Collaborated with the Architecture Working Group to design and establish the GHGA platform, building on existing frameworks and well-established community standards
  • ·Led the Metadata Task Force to design, curate, and maintain the GHGA Metadata Schema, enabling consistent description and discovery of human omics datasets

Feb 2018 – Mar 2021

Berkeley, CA, USA

Staff Software Developer

Lawrence Berkeley National Laboratory
Monarch Initiative
  • ·Contributed to the design and development of the Monarch API, improving access to integrated genotype–phenotype data
  • ·Collaborated with the UI development team to enhance the Monarch web interface and user experience
  • ·Partnered with the data ingest team to explore new strategies for building and improving the integrated Monarch knowledge graph
Gene Ontology
  • ·Extended the scope and functionality of the GO API in collaboration with the development team
  • ·Worked with scientists and developers to apply next-generation GO annotations to model biological systems
Biomedical Data Translator
  • ·Helped define community standards for representing biological and biomedical data as knowledge graphs
  • ·Modeled diverse types of biomedical data and coordinated ETL efforts across the project
  • ·Developed tools for exchanging data between heterogeneous knowledge graph initiatives
  • ·Led the development and evolution of the Biolink Model, a universal schema for knowledge graphs in clinical, biomedical, and translational science
KG-COVID-19
  • ·Built a flexible ETL pipeline for generating a knowledge graph focused on COVID-19 datasets
  • ·Assisted in setting up RDF and Neo4j endpoints for the COVID-19 knowledge graph
  • ·Engaged with researchers to prioritize potential therapeutic targets for COVID-19
  • ·Integrated the COVID-19 knowledge graph into the National COVID Cohort Collaborative (N3C) and the COVID-19 International Research Team (COV-IRT)

Feb 2014 – Feb 2018

Columbia, MO, USA

Research Analyst

University of Missouri

  • ·Development and maintenance of Apollo, a collaborative genome annotation editing tool
  • ·Implementation and maintenance of tools for the Bovine Genome Database and Hymenoptera Genome Database
  • ·Implementation, deployment and maintenance of a data warehouse for Bovine genomics (BovineMine), Hymenoptera genomics (HymenopteraMine), and Maize genetics (MaizeMine)

Aug 2013 – Dec 2013

Atlanta, GA, USA

Graduate Research Assistant

Georgia Institute of Technology

Jun 2013 – Aug 2013

NY, USA

Bioinformatics Intern

Regeneron Pharmaceuticals

Jan 2013 – May 2013

Atlanta, GA, USA

Graduate Research Assistant

Georgia Institute of Technology

Education

2012 – 2013

MS Bioinformatics

Georgia Institute of Technology, USA

2007 – 2011

B. Tech Bioinformatics

Dr. D. Y. Patil Vidyapeeth, Pune, India

Publications

2022

Unni D. R., Moxon S. A. T. et al

Biolink Model: A universal schema for knowledge graphs in clinical, biomedical, and translational science

Clinical and Translational Science, 15(8), 1848–1855

2021

The Gene Ontology Consortium

The Gene Ontology resource: enriching a GOld mine

Nucleic Acids Research, 49(D1), D325–D334

2020

Haendel, M. A., Chute, C. G. et al

The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment

Journal of the American Medical Informatics Association, 28(3), 427–443

Haendel, M. et al

How many rare diseases are there?

Nature Reviews Drug Discovery, 19(2), 77–78

2019

Dunn, N. A. et al

Apollo: Democratizing genome annotation

PLOS Computational Biology, 15(2), e1006790

2018

Biomedical Data Translator Consortium

Toward A Universal Biomedical Data Translator

Clinical and Translational Science, 12(2), 86–90

Biomedical Data Translator Consortium

The Biomedical Data Translator Program: Conception, Culture, and Community

Clinical and Translational Science, 12(2), 91–94

2015

Elsik, C. G. et al

Hymenoptera Genome Database: integrating genome annotations in HymenopteraMine

Nucleic Acids Research, 44(D1), D793–D800

Elsik, C. G. et al

Bovine Genome Database: new tools for gleaning function from the Bos taurus genome

Nucleic Acids Research, 44(D1), D834–D839

© 2026 Deepak Unni