Aug
13
Tue
2013
Plenary Talk: Modeling strategy based on Petri-nets @ Sathyam Hall
Aug 13 @ 9:20 am – 10:00 am

jaapJaap Heringa, Ph.D.
Director & Professor of Bioinformatics, IBIVU VU University Amsterdam, The Netherlands


Modeling strategy based on Petri-nets

In my talk I will introduce a formal modeling strategy based on Petri-nets, which are a convenient means of modeling biological processes. I will illustrate the capabilities of Petri-nets as reasoning vehicles using two examples: Haematopoietic stem cell differentiation in mice, and vulval development in C. elegance. The first system was modeled using a Boolean implementation, and the second using a coarse-grained multi-cellular Petri-net model. Concepts such as the model state space,  attractor states, and reasoning to adapt the model to the biological reality will be discussed.

Invited Talk: Interpretation of Genomic Variation – Identifying Rare Variations Leading to Disease @ Sathyam Hall
Aug 13 @ 10:20 am – 10:40 am

SrinivasanRajgopal Srinivasan, Ph.D.
Principal Scientist & Head Bio IT R&D, TCS Innovation Labs, India


Interpretation of Genomic Variation – Identifying Rare Variations Leading to Disease

Genome sequencing technologies are generating an abundance of data on human genetic variations. A big challenge lies in interpreting the functional relevance of such variations, especially in clinical settings. A first step in understanding the clinical relevance of genetic variations is to annotate the variants for region of occurrence, degree of conservation both within and across species, pattern of variation across related individuals, novelty of the variation and know effects of related variations.  Several tools already exist for this purpose. However, these tools have their strengths and weaknesses. A second issue is the development of algorithms, which, given a rich annotation of variants are able to prioritize the variants as being relevant to the phenotype under investigation.

In my talk I will detail work that has been done in our labs to address both of the above problems. I will also illustrate the application of these tools that helped identify a rare mutation in the ATM gene leading to a diagnosis of AT in two infants.