Biomedical Computing

Graph providing evidence for confirming sibling relationship given matches at single nucleotide polymorphism loci.

Is it possible to correlate clinical outcomes with genomic data? What unique risks does genomic data pose to personal privacy? Guest lecturer Christopher Cassa discusses how single nucleotide polymorphisms (SNPs) could be used to identify sibling genotypes. (Figure from Cassa, Christopher A. et al. "My Sister's Keeper?: Genomic Research and the Identifiability of Siblings." BMC Medical Genomics 1, no. 32 (2008).)


MIT Course Number

HST.950J / 6.872

As Taught In

Fall 2010



Cite This Course

Course Features

Course Description

Analyzes computational needs of clinical medicine reviews systems and approaches that have been used to support those needs, and the relationship between clinical data and gene and protein measurements. Topics: the nature of clinical data; architecture and design of healthcare information systems; privacy and security issues; medical expertsystems; introduction to bioinformatics. Case studies and guest lectures describe contemporary systems and research projects. Term project using large clinical and genomic data sets integrates classroom topics.

Other OCW Versions

OCW has published multiple versions of this subject. Question_OVT logo

Archived versions: Question_avt logo

Peter Szolovits, and Gil Alterovitz. HST.950J Biomedical Computing, Fall 2010. (Massachusetts Institute of Technology: MIT OpenCourseWare), (Accessed). License: Creative Commons BY-NC-SA

For more information about using these materials and the Creative Commons license, see our Terms of Use.