Sentence examples for diseases collections from inspiring English sources

The majority of these samples were chosen from the Chromosomal Aberrations and Heritable Diseases collections.

Many clinical laboratories and research institutes use NIGMS Repository cell lines and/or DNA samples, particularly samples from the Chromosomal Aberrations and Heritable Diseases collections, as standards or reference materials to develop and validate their CMA assays.

Recently, approximately 900 cell lines, mostly chosen from the Chromosomal Aberrations and Heritable Diseases collections, have been further characterized in detail at the Coriell Institute using the Affymetrix Genome-Wide Human SNP Array 6.0 to detect copy number variations and copy number neutral loss of heterozygosity.

In summary, a database containing genomic information for approximately 900 cell lines, which are mostly chosen from the Chromosomal Aberrations Collection and Heritable Diseases Collection of the NIGMS repository and intensively analyzed by karyotype, FISH, and CMA assays at the Coriell Institute, has been constructed.

Anonymized tissue samples remaining after the diagnostic evaluation were used in this project in the context of a study ("Molecular neuropathologic investigation of neurodegenerative diseases"; collection of biological samples named "CJD KIN-Biobank") approved by the Ethics Committee of the Medical University of Vienna (No. 396/2011) and followed the principles of the Declaration of Helsinki.

A large number of plasma samples selected from well characterized psychiatric disease collections were submitted to protein profiling using a commercially available multi-analyte protein panel that contains a number of cytokines, chemokines, neurotrophins and hormones involved in pathways hypothesized to be involved in the pathophysiology of psychiatric diseases.

With larger, and more clearly refined disease collections, our multinomial regression approach thus provides a powerful approach to detect variants contributing to the phenotype overall, whilst also highlighting those that may be specific to one category of disease.

One limitation of this methodology is the fact that although several popular gene variants collections are ongoing (dbSNP has recently passed the 12 million unique human gene variant milestone), a relatively small number of clinically curated and authoritative gene-disease collections exist as used for diagnostic purposes.

Notable collections include those of M. K. Bellue, T. C. Fuller, G. Douglas Barbe, G. F. Hrusa, D. G. Kelch, and G. L. Stout (plant disease collection, BPS).

This editorial introduces the F1000Research rare disease collection.

To date, the Krabbe disease collection within the Biobank includes 36 families.