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DNA sequencing
Towards Accurate Biomedical Genomics Anywhere Anytime - Graduate Seminar
Xin Gao, Program Chair, Computer Science
Feb 17, 12:00
-
13:00
B9 L2 H1 R2322
biomedicine
DNA sequencing
Abstract Current genetic diagnosis by next-generation sequencing requires a large investment of resources and offers little point-of-care portability. Furthermore, it is unable to detect many types of genetic variations - including large deletions, duplications, and balanced translocations - that are relevant to human diseases and health. Comparing to other sequencing technologies, Nanopore sequencing owns the advantages of point-of-care (i.e., sequencing anywhere anytime), long reads (i.e., assembly-free to detect various genetic variations), and PCR free (i.e., sample preparation is easy)
