Immunology Ontologies and Their Applications in Processing Clinical Data

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The National Center for Biomedical Ontology (NCBO) in collaboration with the Protein Ontology (PRO) and the Infectious Disease Ontology (IDO) will host a three-day dissemination workshop in Buffalo, NY on June 11-13, 2012.

Day 1 will provide a survey of current ontology-based research in immunology and infectious disease with a view to future coordination among ontology developers and users in this field.
Day 2 will be focused on flow cytometry, including the question of the Cell and Protein Ontologies and of the role of surface protein expression in cell type classification.
Day 3 will include a session devoted to the use of ontologies to assist clinicians working with infectious disease data, followed by a session on the Ontology for General Medical Science.

Venue:

Days 1 and 2, Ramada Inn, UB North Campus, Buffalo
Day 3: Hauptmann-Woodward Institute, Buffalo

Goals

Provisional goals of the meeting are:

To identify and coordinate activities on-going in immunology ontology and related fields, with special attention to the use of ontologies to support clinical data analysis in flow cytometry and related fields.

Registration

This meeting is free for registered participants. Space is limited and those interested in participating should contact Barry Smith as soon as possible.

Day 1: Monday, June 11, 2012

08:30 Registration and Breakfast

An Overview of Ontologies to Support Research in Immunology and Infectious Disease

Morning: The Gene Ontology, Reactome, The Immunology Ontology, The Immune Epitope Ontology and the Allergy Ontology

09:15 Barry Smith (University at Buffalo) and Cathy Wu (University of Delaware)

Bio-Ontologies for Immunology Research: An Introduction
Brief survey of the goals of the meeting.

09:30 Alexander Diehl (University at Buffalo)

The Gene Ontology and Immune System Processes
The Gene Ontology contains a wealth of terms covering immune system processes for the annotation of proteins involved in the functioning of the immune system. I will provide a overview of these terms and their use in GO annotation.

10:00 Cliburn Chan (Duke University)

Ontology for Cellular Immune Networks
Will describe initial work on an ontology of cellular immune networks that is designed to capture the qualitative cytokine expression patterns and cellular phenotypes associated with specific immune activation networks (e.g. Th1 network). We will outline use of the ontology for immune assay integration and statistical enrichment analysis.

10:30 Break

11:00 Anna Maria Masci (Duke University)

The Immunology Ontology (with special focus on the liver)
An emerging scenario is uncovering immune response as a sophisticated biological process, which requires an intensive cross-talk between immunocytes, parenchymal and stromal cell types. These timely and anatomically restricted interactions regulate the outcome of immune response to damage induced by stress and pathogens. Due to its complexity and patho-physiological relevance, the liver represents an interesting prototype of context-dependent immune response. We will introduce the Liver Immunology Ontology (LIO), which has as primary goal the representation of the immune response induced in the context of the liver.

11:30 Peter d'Eustacho (New York University)

Innate Immunity: Signaling via Toll-Like Receptors in Reactome
The innate immune responses mediated by Toll-like receptors (TLR) provide a first line of defense against microbial pathogens in many vertebrates. In Reactome we have integrated annotations of human TLR molecular functions with those of 6800 other human proteins involved in diverse biological processes to generate a resource suitable for data mining, pathway analysis, and other systems biology approaches. These annotations allow human TLR proteins, the complexes they form, and the functions they mediate to be classified and related to those of structurally similar TLR proteins from chicken, mouse, and other species.

12:00 Lunchtime talk Atul Butte (Stanford)

Discovery of a novel inflammatory receptor and related drug for type 2 diabetes from integration of publicly-available microarray data

13:30 Alexander C. Yu (University at Buffalo)

The Allergy Ontology

14:00 Lindsay Cowell (University of Texas Southwestern Medical Center)

An Introduction to the Infectious Disease Ontology
The IDO-Core; new approach to MIREOTing; new terms/definitions/relations; a template for creating an IDO Extension

14:30 Albert Goldfain (Blue Highway)

Staph Aureus (Sa) IDO

15:00 Break

15:30 Christos (Kitsos) Louis (IMBB-FORTH, Crete)

IDO Mal (Malaria Ontology)

16:00 Yu Lin (University of Michigan)

IDO Bru (Brucellosis Ontology)
IDO Bru is an extension ontology of IDO. We will focus on those aspects of Brucellosis represented in IDOBru as outlined in [1]. We will also discuss IDOBru's policy on use of IDs, and its treatment of Brucella-host interaction.

16:30 Oliver He (University of Michigan)

Contributions of the Vaccine Ontology (VO) to Immunology Research and Public Health
Vaccinology is applied immunology. VO is a community-based biomedical ontology in the domain of vaccine and vaccination. We will introduce the top level of VO, and sketch applications of VO in elucidating fundamental protective immune mechanisms and improving public health.

Day 2: Tuesday, June 12, 2012

Ontologies and Flow Cytometry Informatics

Background Increasingly, flow cytometry is being employed in clinical laboratories for the diagnosis, prognosis and monitoring of disease. The advent of highly multidimensional flow cytometry and automated gating algorithms for the analysis of flow cytometry data, coupled with the rise of personalized medicine, are poised to expand greatly the need for a reliable, structured framework for the representation of the types of cells present in human blood and tissues. We are currently enhancing the representation of hematopoietic and other cell types in the Cell Ontology (CL) to allow for the logical definition of cell types based on cellular attributes, and in doing so we rely on relations to terms of the Protein Ontology (PRO) as a key component of these definitions. The goal of today's session is explore how the use of clinical flow cytometry data can serve as a driver of ontology development in both the PRO and the CL by assessing current standard clinical assays and recent approaches based on automated gating of multidimensional flow cytometry.
Examples of questions to be addressed include:
Which protein isoforms and post-translationally modified forms identified by flow cytometry typing reagents need to be represented in the PRO to enable cell types defined in their terms to be represented in the CL?
How can use of the PRO and CL ontologies will promote standardization in interpretation and integration of clinical flow cytometry data?
Background Reading
The Protein Ontology: a structured representation of protein forms and complexes
Logical Development of the Cell Ontology
Cytometry-Ontology Framework (Draft)

08:30 Breakfast

9:00-noon: Introduction to the Protein Ontology Flow Cytometry Driving Biological Project

9:00 Cathy Wu (University of Delaware): Introduction to the Protein Ontology

9:30 Alexander Diehl (Buffalo)

Hematopoietic Cell Types in the Cell Ontology
The Cell Ontology includes over 350 terms that represent hematopoietic cell types. I will provide an overview of these terms and our strategy for representing key properties of cell types through logical definitions, with examples from Leukemia and Multiple Myeloma

10:00 Discussion of the PRO Driving Biomedical Project Moderator: Lindsay Cowell (University of Texas Southwestern Medical Center)

Presentation of key issues:
Assessing representation requirements for Flow Cytometry in PRO, CL, IEDB, OBI, ImmPort, and Immune System Modeling.
Development of a data store to collect extended cell type-protein relationships.
Defining a tool wish-list for CL-linked flow cytometry analysis and CL-assisted marker selection for cell type analysis.

12:30 Lunch

Afternoon: Automated gating of Flow Cytometry results and linking to the Cell Ontology. Flow cytometry typing of normal and malignant cell types

13:30 Cliburn Chan (Duke)

Automated flow cytometry analysis in HIV studies
Will describe recent work on automated cell subset identification and alignment across multiple HIV-related data sets with statistical mixture models. What do we need in order to be able to use ontologies for automated annotation and labeling of cell subsets?

14:00 Nikesh Kotecha (Cytobank)

Incorporating annotations into the analysis workflow - examples using Cytobank and NCBO's BioPortal

14:30 Dave Parrish (LabAnswer)

Storing and Retrieving Flow Cytometry Data
The Flow Cytometry Laboratory at Roswell Park Cancer Institute has recently deployed an internally developed application managing the operational workflow of the laboratory. We will describe the use of the relational database in capturing assay results and ultimately associating with a final interpretation. Although early in the process the goal is to support the use of the Cell and Protein Ontologies in panel design and interpretation classification.

15:00 Break

15:30 Oliver He (University of Michigan)

How Flow Cytometry can be used in Vaccine Research
To better understand fundamental protective immune mechanisms, flow cytometry has frequently been used to measure vaccine-induced innate immunity, and antigen-specific T-cell and B-cell responses. Biomedical ontologies (e.g., VO, OBI, and PRO) play important roles in data representation, integration, and automated reasoning in vaccine-related flow cytometry research.

16:00 Melanie Courtot (Ryan Brinkman's group, Vancouver)

1. Overview of the representation of flow cytometry assays in OBI
2. Connecting results from automated FCM analysis systems with the Cell Ontology

Day 3: Wednesday, June 13, 2012

Note Wednesday venue is: Hauptmann-Woodward Institute, Buffalo

8:30 Taxis will leave Ramada Hotel

9:00 Breakfast

9:00-noon: Immunology Ontologies (Continued)

9:30 Bjoern Peters (La Jolla Institute for Allergy and Immunology)

Representation of immunology experiments using OBI
Representing epitope mapping experiments for the Immune Epitope Database (IEDB)
The Ontology for Biomedical Investigations (OBI) is an ontology that provides terms with precisely defined meaning to describe all aspects of how biomedical investigations are conducted. OBI builds on the Gene Ontology (GO) and related efforts that provide a formal and interoperable representation of biomedical knowledge. OBI adds the ability to describe how this knowledge was derived. OBI covers all phases of the investigation process, such as planning, execution and reporting. It represents information and material entities that participate in these processes, as well as roles and functions. The presentation will describe the state of OBI and several applications that are using it. Specific focus will be on epitope mapping and characterization experiments captured in the Immune Epitope Database (IEDB) which heavily utilizes OBI. The presentation will also point out gaps in coverage of immunological terms that are currently in OBI but poorly defined and outside the scope of OBI, and which deserve a better home.

10:30 Break

11:00 Alexander Diehl (Buffalo)

Towards an Auto-Immune Disease Ontology
I will discuss the construction of an auto-immune disease ontology through use of the Ontology of General Medical Sciences as a general framework for ontology development.

noon-3pm SESSION OPEN TO THE PUBLIC (includes lunch)

The Role of Ontologies in Clinical Medicine

Albert Goldfain (Blue Highway / Syracuse)
Creating Personalized Infectious Disease Ontologies
Alan Ruttenberg (Buffalo)
The Protein Ontology and the Treatment of Protein Isoforms, Mutations, and Aggregates of Relevance to Alzheimer's Disease
Christos (Kitsos) Louis (IMBB-FORTH, Crete)
Ontologies and Vector-Borne Diseases
Werner Ceusters (Buffalo)
Assessment instruments and biomedical reality: examples in the pain domain

3pm-6pm: Working Session on the Ontology for General Medical Science (OGMS)

Moderator: Albert Goldfain (Blue Highway / Syracuse)
Topics to be treated will include:
Current status of OGMS and the OGMS Reference
Linking diseases to their underlying disorders using basis relations
Defining 'relapse' and 'remission' processes.
Updates on the Vital Sign Ontology
Recipes for OGMS-conformant extension ontologies
Close: 6:00pm

Relevant ontology efforts

GO-IP Gene Ontology -- Immunological Process (Alexander Diehl)
CL Cell ontology immune branches
PRO Protein Ontology
IO Immunology Ontology (Lindsay Cowell and Alexander Diehl)
IEO Immune Epitope Ontology (Bjoern Peters)
MHC Major Histocompatibility Complex Ontology (Bjoern Peters)
OGMS Ontology for General Medical Science (Albert Goldfain)
IDO Infectious Disease Ontology (Lindsay Cowell)
Vaccine Ontology (Oliver He)
AO Allergy Ontology (Alex C. Yu)
ND Neurological Disease Ontology (Alexander Diehl)

Participants will include

Ryan Brinkman (University of British Columbia)
Atul Butte (Stanford University)
James S. Cavenaugh (University of Rochester Medical Center)
Werner Ceusters (University at Buffalo)
Cliburn Chan (Duke University)
Quan Chen (NIH/NIAID)
Melanie Courtot (BCCRC, Vancouver)
Alexander Cox (University at Buffalo)
Lindsay Cowell (University of Texas Southwestern Medical Center)
Oliver Crespo (BD Biosciences, San Jose, CA)
Paresh Dandona (Diabetes and Endocrinology Center of Western New York / University at Buffalo)
Peter d'Eustachio (New York University)
Alexander Diehl (University at Buffalo)
Chester Fox (University at Buffalo)
Lee Ann Garrett-Sinha (University at Buffalo)
Albert Goldfain (University at Buffalo, Syracuse University and Blue Highway, Inc.)
Oliver He (University of Michigan)
Leonard Jacuzzo (University at Buffalo)
Mark Jensen (University at Buffalo)
Christos (Kitsos) Louis (IMBB-FORTH, Crete)
Nikesh Kotecha (Cytobank)
Yu Lin (University of Michigan)
Wei Luo (University at Buffalo)
Supriya Mahajan (University at Buffalo)
Anna Maria Masci (Duke University)
Darren Natale (Georgetown University)
Dave Parrish (Digital Infuzion)
Bjoern Peters (La Jolla Institute for Allergy and Immunology)
Mark Ressler (University at Buffalo)
Jessica L. Reynolds (University at Buffalo)
Alan Ruttenberg (University at Buffalo)
Stanley A. Schwartz (University at Buffalo)
Prontip Saelee (University at Buffalo)
Veronica Shamovsky (NYU School of Medicine)
Barry Smith (University at Buffalo)
Cathy Wu (University of Delaware, Georgetown University)
Alex C. Yu (University at Buffalo)
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