Identifying and Analyzing Indel Variants in the Human Genome Using Computational Approaches
Insertion and deletion (indel), a common form of genetic variation, has been shown to cause or contribute to human genetic diseases and cancer. Despite this importance and being the second most abundant variant type in the human genome, indels have not been studied as much as the single nucleotide p...
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Virginia Tech
2019
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| Online Access: | http://hdl.handle.net/10919/90797 |