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The rest of this article is focused on only multiple global alignments of homologous proteins. The first two are a natural consequence of most representations of alignments and their annotation being human-unreadable and best portrayed in the familiar sequence row and alignment column format, of which examples are widespread in the literature.
The human genome was the first of all vertebrates to be sequenced to such near-completion, and as of 2018, the diploid genomes of over a million individual humans had been determined using next-generation sequencing. [59] These data are used worldwide in biomedical science, anthropology, forensics and other branches of science.
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The Single Nucleotide Polymorphism Database [1] (dbSNP) is a free public archive for genetic variation within and across different species developed and hosted by the National Center for Biotechnology Information (NCBI) in collaboration with the National Human Genome Research Institute (NHGRI).
The following other wikis use this file: Usage on bs.wikipedia.org Gen; Genetika; Usage on el.wikipedia.org Ανθρώπινο γονιδίωμα; Usage on en.wikiquote.org Human genome; Usage on en.wikiversity.org Draft:Original research/Genomics; WikiJournal of Medicine/Medical gallery of Mikael Häggström 2014; Usage on mk.wikipedia.org