Detection of copy number variations in epilepsy using exome data

Detection of copy number variations in epilepsy using exome data

Copy number variations' effect on drug response still overlooked

Copy number variations' effect on drug response still overlooked

Genetics in Medicine - Abstract of article: Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

Expanded genetic screening panel for the Ashkenazi Jewish population : Genetics in Medicine

SNP and copy number variation Databases

SNP and copy number variation Databases

Mitochondrial DNA copy number variation across human cancers

Mitochondrial DNA copy number variation across human cancers

BCM Researchers Reveal Copy Number Variation Could Affect Severity of Genetic Diseases

First comprehensive study of genetic risks for Inflammatory Bowel Disease (IBD) in African-Americans performed.

The Role of mGluR Copy Number Variation in Genetic and Environmental Forms of Syndromic Autism Spectrum Disorder

RANBP1 Gene may link to Autism and other Neuro Disorders

Gene may link to Autism and other Neuro Disorders

One of the most abundant proteins in human saliva, mucin-7, is encoded by the MUC7 gene, which harbors copy number variable subexonic repeats (PTS-repeats) that affect the size and glycosylation potential of this protein. We recently documented the adaptive evolution of MUC7 subexonic copy number variation among primates. Yet, the evolution of MUC7 genetic variation in humans remained unexplored. Here, we found that PTS-repeat copy number variation has evolved recurrently in the human…

One of the most abundant proteins in human saliva, mucin-7, is encoded by the MUC7 gene, which harbors copy number variable subexonic repeats (PTS-repeats) that affect the size and glycosylation potential of this protein. We recently documented the adaptive evolution of MUC7 subexonic copy number variation among primates. Yet, the evolution of MUC7 genetic variation in humans remained unexplored. Here, we found that PTS-repeat copy number variation has evolved recurrently in the human…

A Bayesian Analysis of Copy Number Variations in Array Comparative Genomic Hybridization Data

Array Comparative Genomic Hybridization (CGH) has been widely used for detecting genomic copy number variations (CNVs). The central goal of array CGH data analysis is to .

Pinterest
Search