Related Experiment Video

Updated: Feb 17, 2026

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing
11:02

Detecting Somatic Genetic Alterations in Tumor Specimens by Exon Capture and Massively Parallel Sequencing

Published on: October 18, 2013

20.0K

Digital multiplex ligation-dependent probe amplification identifies exon-level copy number variants in patients with

Ceren Damla Durmaz1, Nesibe Saliha Bulut2, Dilsu Dicle Erkan2

  • 1Department of Medical Genetics, School of Medicine, Hacettepe University, Ankara, Turkey. cdamladurmaz@hotmail.com.

Molecular Biology Reports
|February 16, 2026
PubMed
Abstract

No abstract available in PubMed .

Keywords:
CDKN2ACNVDigital MLPAHereditary cancerLynch syndromeMLH1PMS2

More Related Videos

Detection and Monitoring of Tumor Associated Circulating DNA in Patient Biofluids06:53

Detection and Monitoring of Tumor Associated Circulating DNA in Patient Biofluids

Published on: June 8, 2019

9.2K
Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies13:24

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies

Published on: April 11, 2016

12.3K

Related Concept Videos

Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.8K