A Simulation-based Approach to Study Rare Variant Associations Across the Disease Spectrum
Although complete understanding of the mechanisms of rare genetic variants in disease continues to elude us, Next Generation Sequencing (NGS) has facilitated significant gene discoveries across the disease spectrum. However, the cost of NGS hinders its use for identifying rare variants in common di...
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| Format: | Others |
| Language: | English |
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2013
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| Online Access: | http://hdl.handle.net/1911/71920 |