Microarray analysis identifies more chromosome abnormalities than traditional karyotyping in prenatal testing. Microarrays will also identify findings of unclear clinical significance that should ...

Apart from their use as a tool for diagnostic testing in a broad sense, microarrays have also become a means for molecule production. For real diagnostics, data interpretation is frequently the ...

2 West Midlands Regional Genetics Service, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK Background Identification of CNVs through ...

One of the primary obstacles in microarray-based cancer classification is the disproportionate number of features relative to patient samples, leading to model overfitting and reduced accuracy.

This condition is called triploidy. A fetus with this extra chromosome is said to be unable to survive. Here are the causes ...

ggc.scot.nhs.uk Array-comparative genomic hybridisation (array-CGH) is a relatively new test that permits close scrutiny of chromosomal structure to detect genomic microdeletions and microduplications ...

Parallel quantification of large numbers of messenger RNA transcripts using microarray technology promises to provide detailed insight into cellular processes involved in the regulation of gene ...

Rates of genetic testing for autism and intellectual and development disorders were associated with race, gender, and insurance company.

We have technologies to generate ‘designer’ and ‘beam search’ arrays from particular glycoconjugates to characterise novel recognition systems. We interpret and display the microarray results using ...