This test compares the patient’s sample to a normal control sample to find very small missing or extra chromosome pieces that cannot be seen under a microscope.

This test will detect chromosomal imbalances that could be associated with developmental delay/congenital anomalies. It provides detection of possible uniparental disomy of any …

Aug 15, 2020 · A DNA microarray is a tool used to determine whether the DNA from a particular individual contains a mutation in genes.

Quest helps you harness the power of chromosomal microarray analysis (CMA) Understanding and diagnosing the potential causes of genetic conditions is an essential first step in optimizing …

Aug 20, 2025 · A microarray test is a genetic test that examines a person’s DNA to detect missing or duplicated segments. This laboratory technique provides a comprehensive overview of …

Significance analysis of microarrays (SAM) is a statistical technique, established in 2001 by Virginia Tusher, Robert Tibshirani and Gilbert Chu, for determining whether changes in gene …

Microarrays are versatile tools that analyze thousands of genes or genetic variations at once. They are used to study gene expressions, detect mutations, and identify biomarkers in research.

A chromosomal microarray analysis, also called microarray or array, is a type of genetic test that looks for missing or extra portions of a chromosome. We call these “deletions” or …

A microarray is a laboratory technique used in the study and analysis of biological molecules, particularly DNA and proteins, in which a probe of interest is affixed in a grid pattern to the …

Dec 20, 2023 · The Microarray genetic testing process involves taking a sample of an individual’s DNA, typically from blood or saliva, and submitting it to a laboratory for analysis. The DNA is …