We have updated our Cutis Laxa panel. Visit www.asperbio.com/cutis-laxa-ngs-panel/ to see the new version of the test.
New panel in Asper Cardiogenetics
Published 26/10/2020Left Ventricular Noncompaction Cardiomyopathy panel covers the analysis of 13 genes. Read more at www.asperbio.com/left-ventricular-noncompaction-cardiomyopathy
Updates in Asper Neurogenetics testing menu
Published 21/10/2020We now offer a new test for Congenital Muscular Dystrophy, which covers 29 genes and disease-associated non-coding variants. Cornelia de Lange Syndrome and Limb-Girdle Muscular Dystrophy panels also include the analysis of non-coding variants. In addition, we have added genes to the Limb-Girdle Muscular Dystrophy gene set. Learn more at www.asperbio.com/asper-neurogenetics/
Hereditary ataxia
Published 20/10/2020We have expanded our testing options for different types of hereditary ataxia. NGS panel now covers 148 genes and selected non-coding variants associated with spinocerebellar ataxia, episodic ataxia, and cerebellar ataxia. Repeat expansion analysis is available for 14 genes. CNVs are detected based on sequencing data or by Chromosomal Microarray Analysis. Mitochondrial genome sequencing can also be performed to determine the specific genetic cause of hereditary ataxia. Read more at https://www.asperbio.com/asper-neurogenetics/hereditary-ataxia/