Download PDFOpen PDF in browserSingle nucleotide variation context in human genomeEasyChair Preprint 493 pages•Date: April 6, 2018AbstractWe use the data made available by the 1000 Genomes Project to investigate variation context in the human genome population. We observe that word frequencies in the vicinity of single nucleotide variation (SNV) sites are associated with the type of variation. Keyphrases: Computational genomics, grch37 reference human genome assembly, human genome, single nucleotide variation, single nucleotide variations, variant call
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