Chromosome 21 Pan-acea?

The sequencing of the human genome has great potential to yield insights into the genetic basis of human diseases. Now, a tool has been developed that can unleash this potential on a disease that affects one out of 700 live births: Down syndrome.1 This tool is the Pan® Chromosome 21 Array, a DNA chip for human chromosome 21 that was developed by Ebersberg, Germany-based MWG-Biotech AG in collaboration with the Max Planck Institute for Molecular Genetics. By using this array to compare the ex

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Each known chromosome 21 gene and predicted open reading frame (ORF), identified using MWG-Biotech's non-redundant proprietary database, is represented once in the array by a 40-nucleotide-long oligonucleotide. A total of 498 chromosome 21-specific oligonucleotides are on the array, none of which contains any stretch longer than 15 bases that is homologous to any other sequence in the genome. These oligonucleotides are produced in-house and are quality controlled by MALDI-TOF mass spectrometry. Investigators can purchase the chip alone or as part of a package that includes coursework, an array scanner, and data-analysis software.

According to Horst Donner, head of development for microarrays at MWG-Biotech, both the sequence-specificity of the oligonucleotides on the array, and the automation of the company's array production, increase the sensitivity and reproducibility of these arrays. However, he indicated that the company will not release data on the sensitivity of its arrays until it can develop a quantitative ...

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