Abstract
Genome analysis is the foundation of many scientific and medical discoveries as well as a key pillar of personalized medicine. Any analysis of a genome fundamentally starts with the reconstruction of the genome from its sequenced fragments. This process is called read mapping. One key goal of read mapping is to find the variations that are present between the sequenced genome and reference genome(s) and to tolerate the errors introduced by the genome sequencing process. Read mapping is currently a major bottleneck in the entire genome analysis pipeline because state-of-the-art genome sequencing technologies are able to sequence a genome much faster than the computational techniques that are employed to reconstruct the genome. New sequencing technologies, like nanopore sequencing, greatly exacerbate this problem while at the same time making genome sequencing much less costly.
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