Read Mapping

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There are many ways that we can analyse the genomic sequencing data to identify variants or mutations. One of the, the most obvious solution that we would do would be just sequence and assemble the individual genome from scratch, similar to de novo sequencing, and then assembled back using the assembly methods that we already know, and compare it against the reference genome, and identify places where the variants occur. But computationally, constructing a a genome from scratch takes a lot of memory and computational power.

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