array comparative genomic hybridization

You are here

We recommend to visit

This is a pilot study, intending to describe the carriers of hereditary disease analysing genomic structural variations of the healthy Lithuanians. Array comparative genomic hybridization method was used to describe DNA copy number variations (CNVs) of the healthy population (73 males, and 73 females). The data was collected during the project PROGENET accomplished by Vilnius University department of Human and Medical Genetics.

EN
© 2024, Lithuanian Society of Laboratory Medicine
randomness