BioE Seminar Series

Mar 10

Thursday, March 10, 2016

4:30 pm - 5:30 pm
Fitzpatrick Center Schiciano Auditorium Side B

Presenter

Sai Reddy, Ph.D. Assistant Professor, Department of Biosystems Science & Engineering ETH Zurich

High-throughput sequencing of immunoglobulin repertoires (Ig-seq) enables unprecedented quantitative analysis of adaptive immunity and thereby offers the potential to revolutionize research in immunobiology, vaccine profiling, and monoclonal antibody engineering. It has long been possible to measure humoral (antibody) immunity through conventional serological assays (e.g., ELISA). However, the ability to obtain quantitative information regarding the molecular diversity and distribution of antibody responses has only recently become possible through Ig-seq. However, Ig-seq is compromised by the presence of bias and errors introduced during library preparation and sequencing and thus prevents reliable immunological conclusions from being made. To overcome this, we have developed an integrated experimental-bioinformatic method known as molecular amplification fingerprinting (MAF), which combines single molecule and amplicons labeling with unique molecular identifiers. By applying MAF-based bioinformatic tools we were able to achieve 98-100% error and bias correction in Ig-seq. We then applied this approach of accurate Ig-seq in order to probe the relationship between antibody genotype and phenotype in a large-scale systems vaccinology study in mice. Finally, by applying multivariate and statistical modeling methods, we were able to predict the immune status of mice based sibased simply on Ig-seq measurements. This extensive systems-based analysis demonstrates how Ig-seq provides

Contact

King, Pamela
681-3927
pamela.king@duke.edu