After sequencing, the data are analyzed to identify mutations, such as single-nucleotide polymorphisms (SNPs), insertions, deletions, and other genomic alterations that might be significant for disease [ 40 ].
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After sequencing, the data are analyzed to identify mutations, such as single-nucleotide polymorphisms (SNPs), insertions, deletions, and other genomic alterations that might be significant for disease [ 40 ].