2 Matching Annotations
  1. Sep 2021
    1. To identify early embryonic base substitutions, we analysed whole-genome sequences of blood samples from 279 individuals with breast cancer (mean sequencing coverage 32-fold; Supplementary Table 1) seeking mutations with VAFs ranging from 10% to 35%

      This is what the research is studying.

  2. Sep 2017
    1. Major flaws in "Identification of individuals by trait prediction using whole-genome sequencing data"

      re Venter study in PNAS, claiming to be able to identify people based on whole genome data