Precise detection of de novo single nucleotide variants in human genomes [Genetics]

The precise determination of de novo genetic variants has enormous implications across different fields of biology and medicine, particularly personalized medicine. Currently, de novo variations are identified by mapping sample reads from a parent–offspring trio to a reference genome, allowing for a certain degree of differences. While widely used, this...

from Genetics via xlomafota13 on Inoreader https://ift.tt/2IWDBCb
via IFTTT