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Constructed and verified a new method that may help detect genomic rearrangements.

Analyzed microRNA expression profiles of lymphoma cells and normal B cells.

Developed an approach to predict how small molecules can modulate biological functions.

Identified candidate inhibitors of histone deacetylases that may play a role in cancer.

Evaluated vision system models for use in genome sequencing.

Developed and optimized methods for purifying Txnip proteins, which may lead to key biological insights.

Studied the association of QT interval duration with common genetic variation.