Only a few cytogenetic and genetic studies have been performed in gastric cancer patients in young age groups. In the present study we used the comparative genomic hybridisation (CGH) method to ...
Human genomes exhibit segmental copy number variation (CNV) at thousands of loci. Rare and de novo deletions and duplications, which are often large (hundreds of kilobases in length), are known risk ...
Pleomorphic xanthoastrocytoma (PXA) poses a diagnostic challenge. The present study relies on methylation-based predictions and focuses on copy number variations (CNV) in PXA. We identified 551 tumors ...
How to copy expressions without changing cell references in Excel Your email has been sent Image: AndreyPopov, Getty Images/iStockphoto Must-read Windows coverage CrowdStrike Outage Disrupts Microsoft ...
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