De novo mutations — sequence variants that are present in a child but absent from both parents — are an important
source of human genetic variation.
Not exact matches
An open -
source C / C + + library
of analytical tools for
human genetic variation data from whole - exome and whole - genome studies.
Our study outlines the major
sources of genetic and phenotypic
variation in iPS cells and establishes their suitability as models
of complex
human traits and cancer.