Company
Genome Diagnostics
with State of the Art Manufacturing Facilities at Parwanoo the Foot hills of the Legend Himalayas. Majority of our assays are CE marked. Quality assurance
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Company
with State of the Art Manufacturing Facilities at Parwanoo the Foot hills of the Legend Himalayas. Majority of our assays are CE marked. Quality assurance
Product
Technology
A molecular cytogenetic method combining chromosomal comparative genomic hybridization technique and microarray to detect chromosomal aberrations and changes in DNA copy numbers in the genome, using oligonucleotides immobilized on a solid support as targets for hybridization.
Technology
Comparative genomic hybridization (CGH) is a technique that allows the detection of losses and gains in DNA copy number across the entire genome without prior knowledge of specific chromosomal abnormalities. Comparative genomic hybridization utilizes the hybridization of differentially labeled tumor and reference DNA to generate a map of DNA copy number changes in tumor genomes. Comparative genomic hybridization is an ideal tool for analyzing chromosomal imbalances in archived tumor material and for examining possible correlations between these findings and tumor phenotypes. (from Ried et al. J Mol Med 1997 75:801-14)
Company
in Thousand Oaks, California, that manufactures Peptide Nucleic Acid (PNA) reagents and CRISPR/Cas9 genome-editing tools for life science research.
Technology
Analysis that looks for differences in the lengths of microsatellite repeats between alleles. Polymorphic microsatellites are present in the genome every few thousand base pairs and can function as molecular markers.
Technology
Any technique designed to amplify a limited genomic DNA sample so as to generate a new sample that is indistinguishable from the original but with a higher DNA concentration.
Technology
A procedure that can determine the DNA sequence for nearly the entire genome of an individual.
Glossary Term
A chromosome not involved in sex determination. The diploid human genome consists of a total of 46 chromosomes which includes 22 pairs of autosomes.
Article
Research record from Genome Med, 2026-07-27. PMID 42509573.
Glossary Term
Variation in the number of copies of a particular sequence within the genetic material of an individual. Large-scale copy number polymorphisms are common and widely distributed in the human genome.
Glossary Term
The complete set of epigenetic modifications on the genome of a cell.