Dennis Lal 1,2,3,4, Ignacio F. Mata 1 on behalf of the Latin American Research consortium on the Genetics of Parkinson’s Disease (LARGE-PD) Genomic Medicine Institute, Cleveland Clinic, Cleveland, OH ...
HBV Pre-S deletion mutation analysis: A high resolution diagnosis method. Regulation of COX-2 expression and epithelial-to-mesenchymal transition by hypoxia-inducible factor-1 alphais associated with ...
FRAMINGHAM, Mass.--(BUSINESS WIRE)--Variantyx, a leader in genomic precision medicine, today announced the launch of its IriSight™ CNV Analysis - a whole genome-based test for the detection of ...
Although array comparative genomic hybridization (aCGH) is currently established as the gold standard for copy number variation (CNV) detection, next-generation sequencing (NGS) is increasingly being ...
Targeting ER-Golgi homeostasis as a therapeutic strategy in lung cancer. Background: In the routine diagnostic of cancers, the monitoring of the transcriptome and the chromosomal abnormalities becomes ...
Copy number variant (CNV) analysis has been part of clinical diagnostics for almost two decades. With the evolution of genomic technologies for CNV detection, we have learned that CNVs can range in ...
Oxford Gene Technology (OGT), The Molecular Genetics Company, held an exclusive workshop exploring the power of exon-focused microarrays in enhancing genetic syndrome research at the recent European ...
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