HST.950J | Fall 2010 | Graduate

Biomedical Computing

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Description:

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).

Alt text:
Graph providing evidence for confirming sibling relationship given matches at single nucleotide polymorphism loci.
Caption:
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).)
Credit:
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).
Graph providing evidence for confirming sibling relationship given matches at single nucleotide polymorphism loci.
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