Lindsay Cowell, PhD

Assistant Professor
Department of Clinical Sciences

Contact Information

UT Southwestern Medical Center
5323 Harry Hines Boulevard
Dallas, Texas 75390

lindsay.cowell@utsouthwestern.edu

Biography

Dr. Cowell received a MS in Biomathematics with a minor in Mathematics in 1995 from North Carolina State University.  In 2000, she received a PhD in Biomathematics with a minor in Immunology, also from North Carolina State University.  She spent three years as a postdoctoral fellow in the Department of Immunology at Duke University Medical Center and then became an Assistant Professor in the Department of Biostatistics and Bioinformatics.  She was also on the gratduate faculty for the Computational Biology and Bioinformatics Graduate Program. In September 2010, she joined the Biomedical Informatics Division in the Department of Clinical Sciences at UT Southwestern.

Dr. Cowell has built a research program focused on the development of bioinformatics and computational biology methods for the study of the immune system and infectious diseases.  In particular, her work has focussed on the somatic diversification of antigen receptor-encoding genes and the development of computable representations of biological and clinical information.  Within each of these areas, she has developed projects that emphasize methodologic development as well as projects focused on answering specific biological questions. 

Dr. Cowell’s research on the somatic diversification of antigen receptor-encoding genes has included projects focused on:

  • the somatic hypermutation of immunoglobulin genes,
  • receptor editing of immunoglobulin genes, and
  • V(D)J recombination.

Her group is currently developing a suite of computational methods for the analysis of antigen receptor repertoires in the context of a variety of disease types, with a current focus on multiple sclerosis. The group is developing RepServer, a web-accessible repertoire analysis server. RepServer will provide a data management infrastructure and a suite of interoperable repertoire analysis tools with an interface that allows users to upload a set of sequences and pass them through a seamless workflow that executes all steps in the analysis and generates an analysis report complete with data summary tables, statistical analyses, figures, and workflow logs.  This project is a collaboration with Dr. Nancy Monson and Richard Scheuermann at UTSW.

Dr. Cowell’s research on the development of computable representations of biological and clinical information has focused on developing methods for the representation of qualitative descriptions of immune responses and infectious diseases and for the use of such representations to enhance algorithms for the analysis of high-throughput data, for the integration of data from disparate resources, and for logical inferencing.  Specific projects within this area have included:

  • the development of a method for representing cell types that is optimized for the analysis of flow cytometry data,
  • application of the method to the representation of cells of hematopoietic lineage,
  • the development of an Infectious Disease Ontology,
  • the development of an extension to the Infectious Disease Ontology for Staphylococcus aureus infections,
  • application of the S. aureus ontology to the development of procedures for the automatic generation and versioning of case report forms,
  • application of the S. aureus ontology to the design of databases and data integration procedures for the integration of data from studies on the role of bacterial virulence.

Education

Graduate SchoolNorth Carolina State University at Raleigh (2000)
Graduate SchoolNorth Carolina State University at Raleigh (1995)
UndergraduateUniversity of North Carolina at Chapel Hill, Education (1992)

Research Interests

Antigen receptor repertoire analysis
Development of biomedical ontologies, particularly for the infectious disease domain
Natural language processing
Somatic diversification of antigen receptor encoding genes

Publications

Featured
Conserved cryptic recombination signals in Vkappa gene segments are cleaved in small pre-B cells.

Lieberman AE, Kuraoka M, Davila M, Kelsoe G, Cowell LG, BMC immunology, 2009 ; 10:37

Featured
An improved ontological representation of dendritic cells as a paradigm for all cell types.

Masci AM, Arighi CN, Diehl AD, Lieberman AE, Mungall C, Scheuermann RH, Smith B, Cowell LG, BMC bioinformatics, 2009 ; 10:70

Featured
Multiple, conserved cryptic recombination signals in VH gene segments: detection of cleavage products only in pro B cells.

Davila M, Liu F, Cowell LG, Lieberman AE, Heikamp E, Patel A, Kelsoe G, The Journal of experimental medicine, 2007 Dec; 204 (13):3195-208

Featured
Prospective estimation of recombination signal efficiency and identification of functional cryptic signals in the genome by statistical modeling.

Cowell LG, Davila M, Yang K, Kepler TB, Kelsoe G, The Journal of experimental medicine, 2003 Jan; 197 (2):207-20

Featured
Identification and utilization of arbitrary correlations in models of recombination signal sequences.

Cowell LG, Davila M, Kepler TB, Kelsoe G, Genome biology, 2002 ; 3 (12):RESEARCH0072

Featured
The distribution of variation in regulatory gene segments, as present in MHC class II promoters.

Cowell LG, Kepler TB, Janitz M, Lauster R, Mitchison NA, Genome research, 1998 Feb; 8 (2):124-34

Hematopoietic cell types: prototype for a revised cell ontology.

Diehl AD, Augustine AD, Blake JA, Cowell LG, Gold ES, Gondré-Lewis TA, Masci AM, Meehan TF, Morel PA, Nijnik A, Peters B, Pulendran B, Scheuermann RH, Yao QA, Zand MS, Mungall CJ, Journal of biomedical informatics, 2011 Feb; 44 (1):75-9

Towards an ontological representation of resistance: the case of MRSA.

Goldfain A, Smith B, Cowell LG, Journal of biomedical informatics, 2011 Feb; 44 (1):35-41

Logical development of the cell ontology.

Meehan TF, Masci AM, Abdulla A, Cowell LG, Blake JA, Mungall CJ, Diehl AD, BMC bioinformatics, 2011 ; 12:6

Memory B cells from a subset of treatment-naïve relapsing-remitting multiple sclerosis patients elicit CD4(+) T-cell proliferation and IFN-? production in response to myelin basic protein and myelin oligodendrocyte glycoprotein.

Harp CT, Ireland S, Davis LS, Remington G, Cassidy B, Cravens PD, Stuve O, Lovett-Racke AE, Eagar TN, Greenberg BM, Racke MK, Cowell LG, Karandikar NJ, Frohman EM, Monson NL, European journal of immunology, 2010 Oct; 40 (10):2942-56