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Perlegen Sciences high-density oligonucleotide arrays
High Density Oligonucleotide Arrays, supplied by Perlegen Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/oligonucleotide+array/high+density+oligonucleotide+arrays/us08785128-90-16-19
Average 90 stars, based on 1 article reviews
high-density oligonucleotide arrays - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

other:

Article Title: Association of Genetic Polymorphisms With Hepatitis C Virus-related Liver Cirrhosis in Japan
Article Snippet: A GWAS was performed with high-density oligonucleotide arrays (Perlegen Sciences, Santa Clara, CA, USA) for SNP genotyping.

Article Title: Rice Molecular Breeding Laboratories in the Genomics Era: Current Status and Future Considerations
Article Snippet: The technology being used for SNP discovery is hybridization to very high-density oligomer arrays pioneered by Perlegen Sciences, Inc. (Mountain View, Ca 94043, USA).

Article Title: Gene-based Hardy-Weinberg equilibrium test using genotype count data: application to six types of cancers.
Article Snippet: Patients with 11 diseases (heart failure, myocardial infarction, unstable angina, stable angina, arrhythmia, peripheral arterial disease, cerebral aneurysm, cerebral infarction, bronchial asthma, pulmonary emphysema, interstitial lung disease): 2,137 individuals in total genotyped using the Perlegen Sciences high-density oligonucleotide arrays platform, the same platform used for the analysis of cancers other than esophageal cancer.

Article Title: Low LDL Cholesterol Is Not an Independent Risk Factor for Hepatic Steatosis.
Article Snippet: Background Genetic mutations causing defective VLDL secretion and low LDL cholesterol are associated with hepatic steatosis and nonalcoholic fatty liver disease (NAFLD).. Aims Determine if low LDL cholesterol (< 5th percentile) was an independent predictor of hepatic steatosis.. Methods Secondary data analysis of the Dallas Heart study (an urban, multiethnic, probability-based sample), we defined hepatic steatosis utilizing intrahepatic triglyceride (IHTG) analyzed using magnetic resonance spectroscopy in conjunction and available demographic, serological and genetic information.

Article Title: Association of Genetic Polymorphisms With Hepatitis C Virus-related Liver Cirrhosis in Japan
Article Snippet: A GWAS was performed with high-density oligonucleotide arrays (Perlegen Sciences, Santa Clara, CA, USA), resulting in the selection of 233,820 SNPs for genotyping, at the first stage.

Construct:

Article Title: Host genetics affect susceptibility to invasive aspergillosis.
Article Snippet: .. These maps will be constructed within approximately two years using high-throughput DNA sequencing on oligonucleotide microwafer arrays as described recently by Perlegen [Science 294, 1719 (2001)]. ..

DNA Sequencing:

Article Title: Host genetics affect susceptibility to invasive aspergillosis.
Article Snippet: .. These maps will be constructed within approximately two years using high-throughput DNA sequencing on oligonucleotide microwafer arrays as described recently by Perlegen [Science 294, 1719 (2001)]. ..

Control:

Article Title: A powerful method to integrate genotype and gene expression data for dissecting the genetic architecture of a disease.
Article Snippet: .. About 440K SNPs, genotyped using high density oligonucleotide arrays by Perlegen Sciences (Mountain View, CA, USA) passed data quality control checks for all individuals. ..

Hybridization:

Article Title: Single nucleotide polymorphisms: discovery, detection and analysis.
Article Snippet: 10.1517/17410541.2.2.111 © 2 Single nucleotide polymorphisms (SNPs) are the most abundant and simple form of DNA variation.. Analyses of SNPs in the human population have the potential to greatly improve human health, both by predicting susceptibility to disease and guiding choice of therapy.. This review describes new tools for SNP discovery, and current and emerging technologies for large-scale SNP analysis, as well as providing a guide to choosing the best approach for SNP analysis.

Mass Spectrometry:

Article Title: Single nucleotide polymorphisms: discovery, detection and analysis.
Article Snippet: 10.1517/17410541.2.2.111 © 2 Single nucleotide polymorphisms (SNPs) are the most abundant and simple form of DNA variation.. Analyses of SNPs in the human population have the potential to greatly improve human health, both by predicting susceptibility to disease and guiding choice of therapy.. This review describes new tools for SNP discovery, and current and emerging technologies for large-scale SNP analysis, as well as providing a guide to choosing the best approach for SNP analysis.



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