Single nucleotide variation context in human genome

EasyChair Preprint 49

Abstract

We 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

@booklet{EasyChair:49,
  author    = {Vera Enes and João Manuel Rodrigues and Vera Afreixo},
  title     = {Single nucleotide variation context in human genome},
  doi       = {10.29007/mk44},
  howpublished = {EasyChair Preprint 49},
  year      = {EasyChair, 2018}}