About: SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery

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About: SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery Goto Sponge NotDistinct Permalink

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scientific article published on 01 June 2002

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в червні 2002 (uk) im Juni 2002 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en xunu de 2002 (ast) scientific article published on 01 June 2002 (en)
publication date	wds:Q74359356-7AE8C5D6-BF6F-4443-A843-76CCE84A620C
publication date	2002-06-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q74359356-123D6D98-8C7C-4503-9D77-8B0ECB19851E wds:Q74359356-1A95456C-B604-42F2-B8D6-0AFC8901C94E wds:Q74359356-3AABCAE1-284E-43D6-AE8F-DBEDC6F76B65 wds:Q74359356-3C42F9BE-F1C4-471C-884F-846C3855DC3B wds:Q74359356-3C5C7A23-529E-4C0A-A92C-CCCB95B5672D wds:Q74359356-3DA1F334-E3EF-40F8-977A-C5A58C03F563 wds:Q74359356-42DCCBB8-AC6E-4A08-BA45-7240135BD3DB wds:Q74359356-5E0EFC83-D25C-44CB-AFA8-AC6BED24473C wds:Q74359356-7D1B47E8-9C99-4516-9FFF-1C6B7C390ECD wds:Q74359356-81F46B1C-79E7-4344-8A62-2AB91FE03E36 wds:Q74359356-8C02187B-DEE0-4668-A7AC-27AA3F38F22A wds:Q74359356-C2623FD1-1272-4785-9366-0DCC7F0A0936 wds:Q74359356-D0720C77-6EC0-413D-8978-CF9CE6E31929
author name string	Craig A Gelfand Mark Pohl Michael T Boyce-Jacino Shobha Varde Xiaojian Zhao Peter A Bell Renbin Zhao Ching Yu Huang Azzam Yassen Frank Modica Michael Kochersperger Rafael Kopla Surendra Chaturvedi
rdfs:label	SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (en) SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (nl)
skos:prefLabel	SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (en) SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (nl)
name	SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (en) SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (nl)
title	wds:Q74359356-84CA39CA-B516-4808-BFF8-6CCAC6B0C489
title	SNPstream UHT: ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery (en)
page(s)	wds:Q74359356-BAC1525A-9FF4-4301-AD8C-9276721D85BE
page(s)	70-2, 74, 76-7
instance of	wds:Q74359356-D00460EA-0B29-4A4C-AB5C-8D5F9C6749ED
instance of	scholarly article
main subject	wds:Q74359356-615D6B17-036F-4C1D-B97B-797B1C6C0522 wds:Q74359356-F541E77E-C8B2-459C-AAAF-9C3CC2DA56B4
main subject	drug discovery pharmacogenomics
PubMed ID	wds:Q74359356-5204A9F1-C253-4008-B546-2A59A19DB30C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12083401
PubMed ID	12083401
published in	wds:Q74359356-3382515F-7401-4221-8BCF-D2E1151B82EC
published in	BioTechniques
volume	wds:Q74359356-22ADEB43-ADD8-4A8E-97FE-0CB7E9A33FB4
volume	Suppl
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74359356
is cites work of	Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus Genetic mapping in a natural population of collared flycatchers (Ficedula albicollis): conserved synteny but gene order rearrangements on the avian Z chromosome Machine-learning approaches for classifying haplogroup from Y chromosome STR data Development of a single tube 640-plex genotyping method for detection of nucleic acid variations on microarrays Genetic variation in the familial Mediterranean fever gene (MEFV) and risk for Crohn's disease and ulcerative colitis A multiplex allele-specific primer extension assay for forensically informative SNPs distributed throughout the mitochondrial genome Asthma and genes encoding components of the vitamin D pathway Auto-validation of fluorescent primer extension genotyping assay using signal clustering and neural networks Common variants in the NLRP3 region contribute to Crohn's disease susceptibility Computational and experimental approaches to reveal the effects of single nucleotide polymorphisms with respect to disease diagnostics Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations An automated approach to salt selection for new unique trazodone salts Gene mapping in the wild with SNPs: guidelines and future directions. Basic principles and technologies for deciphering the genetic map of cancer. Slow inbred lines of Drosophila melanogaster express as much inbreeding depression as fast inbred lines under semi-natural conditions High-density single-nucleotide polymorphism maps of the human genome. Human leukocyte antigen class I region single-nucleotide polymorphisms are associated with leprosy susceptibility in Vietnam and India A candidate gene study of the type I interferon pathway implicates IKBKE and IL8 as risk loci for SLE. Missing call bias in high-throughput genotyping Silhouette scores for assessment of SNP genotype clusters Polymorphisms in DNA repair genes, smoking, and pancreatic adenocarcinoma risk A low-cost open-source SNP genotyping platform for association mapping applications. Alleles of the NRAMP1 gene are risk factors for pediatric tuberculosis disease Can balancing selection on MHC loci counteract genetic drift in small fragmented populations of black grouse? Genetic and functional analysis of common MRC1 exon 7 polymorphisms in leprosy susceptibility Comparison of GenFlex Tag Array and Pyrosequencing in SNP Genotyping Matrix-assisted laser desorption/ionisation, time-of-flight mass spectrometry in genomics research A genetic risk variant for myocardial infarction on chromosome 6p24 is associated with impaired central hemodynamic indexes Association between polymorphisms in the renin-angiotensin-aldosterone system genes and essential hypertension in the Han Chinese population CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup High-throughput SNP discovery and genotyping for constructing a saturated linkage map of chickpea (Cicer arietinum L.). Fine-scale linkage disequilibrium mapping of age-related macular degeneration in the complement factor H gene region Variants in scavenger receptor class B type I gene are associated with HDL cholesterol levels in younger women Host genotype and tumor phenotype of chemokine decoy receptors integrally affect breast cancer relapse A comprehensive examination of CYP19 variation and risk of breast cancer using two haplotype-tagging approaches Comparative genome mapping among Picea glauca, P. mariana × P. rubens and P. abies, and correspondence with other Pinaceae SNP genotyping to screen for a common deletion in CHARGE syndrome Pseudo-backcrossing design for rapidly pyramiding multiple traits into a preferential rice variety Detecting imbalanced expression of SNP alleles by minisequencing on microarrays Association of a genetic risk score with prevalent and incident myocardial infarction in subjects undergoing coronary angiography Single PCR multiplex SNaPshot reaction for detection of eleven blood group nucleotide polymorphisms: optimization, validation, and one year of routine clinical use Expression quantitative trait loci and receptor pharmacology implicate Arg1 and the GABA-A receptor as therapeutic targets in neuroblastoma.

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