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Whole-genome Sequencing Impact Factor | Open Access Journals
Clinical Infectious Diseases: Open Access

Clinical Infectious Diseases: Open Access

ISSN: 2684-4559

Open Access

Whole-genome Sequencing Impact Factor

Entire genome sequencing ought not be mistaken for DNA profiling, which just decides the probability that hereditary material originated from a specific individual or gathering, and doesn't contain extra data on hereditary connections, beginning or powerlessness to explicit diseases. what's more, entire genome  sequencing ought not be mistaken for techniques that grouping explicit subsets of the genome such strategies incorporate entire exome sequencing (1-2% of the genome) or SNP genotyping (<0.1% of the genome). Starting at 2017 there were no finished genomes for any vertebrates, including people. Between 4% to 9% of the human genome, for the most part satellite DNA, had not been sequenced.

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