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000155333 005__ 20240209132447.0
000155333 0247_ $$2doi$$a10.1016/j.neurobiolaging.2014.07.028
000155333 0247_ $$2pmid$$apmid:25444595
000155333 0247_ $$2pmc$$apmc:PMC4317375
000155333 0247_ $$2ISSN$$a0197-4580
000155333 0247_ $$2ISSN$$a1558-1497
000155333 037__ $$aDZNE-2021-00600
000155333 041__ $$aEnglish
000155333 082__ $$a610
000155333 1001_ $$aNalls, Mike A$$b0
000155333 245__ $$aNeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases.
000155333 260__ $$aAmsterdam [u.a.]$$bElsevier Science$$c2015
000155333 3367_ $$2DRIVER$$aarticle
000155333 3367_ $$2DataCite$$aOutput Types/Journal article
000155333 3367_ $$0PUB:(DE-HGF)16$$2PUB:(DE-HGF)$$aJournal Article$$bjournal$$mjournal$$s1707481436_2407
000155333 3367_ $$2BibTeX$$aARTICLE
000155333 3367_ $$2ORCID$$aJOURNAL_ARTICLE
000155333 3367_ $$00$$2EndNote$$aJournal Article
000155333 520__ $$aOur objective was to design a genotyping platform that would allow rapid genetic characterization of samples in the context of genetic mutations and risk factors associated with common neurodegenerative diseases. The platform needed to be relatively affordable, rapid to deploy, and use a common and accessible technology. Central to this project, we wanted to make the content of the platform open to any investigator without restriction. In designing this array we prioritized a number of types of genetic variability for inclusion, such as known risk alleles, disease-causing mutations, putative risk alleles, and other functionally important variants. The array was primarily designed to allow rapid screening of samples for disease-causing mutations and large population studies of risk factors. Notably, an explicit aim was to make this array widely available to facilitate data sharing across and within diseases. The resulting array, NeuroX, is a remarkably cost and time effective solution for high-quality genotyping. NeuroX comprises a backbone of standard Illumina exome content of approximately 240,000 variants, and over 24,000 custom content variants focusing on neurologic diseases. Data are generated at approximately $50-$60 per sample using a 12-sample format chip and regular Infinium infrastructure; thus, genotyping is rapid and accessible to many investigators. Here, we describe the design of NeuroX, discuss the utility of NeuroX in the analyses of rare and common risk variants, and present quality control metrics and a brief primer for the analysis of NeuroX derived data.
000155333 536__ $$0G:(DE-HGF)POF4-899$$a899 - ohne Topic (POF4-899)$$cPOF4-899$$fPOF IV$$x0
000155333 588__ $$aDataset connected to CrossRef, PubMed, , Journals: pub.dzne.de
000155333 650_7 $$2Other$$aGenetics
000155333 650_7 $$2Other$$aGenotyping
000155333 650_7 $$2Other$$aImputation
000155333 650_7 $$2Other$$aMeta-analysis
000155333 650_7 $$2Other$$aMethods
000155333 650_7 $$2Other$$aNeurodegeneration
000155333 650_7 $$2Other$$aParkinson's
000155333 650_2 $$2MeSH$$aAlleles
000155333 650_2 $$2MeSH$$aCosts and Cost Analysis
000155333 650_2 $$2MeSH$$aGenetic Association Studies: methods
000155333 650_2 $$2MeSH$$aGenetic Predisposition to Disease: genetics
000155333 650_2 $$2MeSH$$aGenetic Variation
000155333 650_2 $$2MeSH$$aGenotyping Techniques: economics
000155333 650_2 $$2MeSH$$aGenotyping Techniques: methods
000155333 650_2 $$2MeSH$$aNeurodegenerative Diseases: genetics
000155333 650_2 $$2MeSH$$aOligonucleotide Array Sequence Analysis: methods
000155333 7001_ $$aBras, Jose$$b1
000155333 7001_ $$0P:(DE-2719)2812102$$aHernandez, Dena G$$b2$$udzne
000155333 7001_ $$aKeller, Margaux F$$b3
000155333 7001_ $$aMajounie, Elisa$$b4
000155333 7001_ $$aRenton, Alan E$$b5
000155333 7001_ $$aSaad, Mohamad$$b6
000155333 7001_ $$0P:(DE-2719)2813349$$aJansen, Iris$$b7$$udzne
000155333 7001_ $$aGuerreiro, Rita$$b8
000155333 7001_ $$aLubbe, Steven$$b9
000155333 7001_ $$aPlagnol, Vincent$$b10
000155333 7001_ $$aGibbs, J Raphael$$b11
000155333 7001_ $$0P:(DE-2719)9000366$$aSchulte, Claudia$$b12$$udzne
000155333 7001_ $$aPankratz, Nathan$$b13
000155333 7001_ $$aSutherland, Margaret$$b14
000155333 7001_ $$aBertram, Lars$$b15
000155333 7001_ $$aLill, Christina M$$b16
000155333 7001_ $$aDeStefano, Anita L$$b17
000155333 7001_ $$aFaroud, Tatiana$$b18
000155333 7001_ $$aEriksson, Nicholas$$b19
000155333 7001_ $$aTung, Joyce Y$$b20
000155333 7001_ $$aEdsall, Connor$$b21
000155333 7001_ $$aNichols, Noah$$b22
000155333 7001_ $$aBrooks, Janet$$b23
000155333 7001_ $$aArepalli, Sampath$$b24
000155333 7001_ $$aPliner, Hannah$$b25
000155333 7001_ $$aLetson, Chris$$b26
000155333 7001_ $$0P:(DE-2719)2810728$$aHeutink, Peter$$b27$$udzne
000155333 7001_ $$aMartinez, Maria$$b28
000155333 7001_ $$0P:(DE-2719)2320009$$aGasser, Thomas$$b29$$udzne
000155333 7001_ $$aTraynor, Bryan J$$b30
000155333 7001_ $$aWood, Nick$$b31
000155333 7001_ $$aHardy, John$$b32
000155333 7001_ $$aSingleton, Andrew B$$b33
000155333 7001_ $$0P:(DE-HGF)0$$aConsortium, International Parkinson's Disease Genomics$$b34$$eCollaboration Author
000155333 7001_ $$0P:(DE-HGF)0$$aconsortium, Parkinson's Disease meta-analysis$$b35$$eCollaboration Author
000155333 7001_ $$aNalls, Mike A$$b36
000155333 7001_ $$aPlagnol, Vincent$$b37
000155333 7001_ $$0P:(DE-2719)2812102$$aHernandez, Dena G$$b38$$udzne
000155333 7001_ $$aEdsall, Connor$$b39
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000155333 7001_ $$aSheerin, Una-Marie$$b42
000155333 7001_ $$aSaad, Mohamad$$b43
000155333 7001_ $$aSimón-Sánchez, Javier$$b44
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000155333 7001_ $$aLesage, Suzanne$$b46
000155333 7001_ $$aSveinbjörnsdóttir, Sigurlaug$$b47
000155333 7001_ $$aArepalli, Sampath$$b48
000155333 7001_ $$aBarker, Roger$$b49
000155333 7001_ $$aBen-Shlomo, Yoav$$b50
000155333 7001_ $$aBerendse, Henk W$$b51
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000155333 7001_ $$aBhatia, Kailash$$b53
000155333 7001_ $$ade Bie, Rob M A$$b54
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000155333 7001_ $$aBloem, Bas$$b56
000155333 7001_ $$aBochdanovits, Zoltan$$b57
000155333 7001_ $$aBonin, Michael$$b58
000155333 7001_ $$aBras, Jose M$$b59
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000155333 7001_ $$aBrooks, Janet$$b61
000155333 7001_ $$aBurn, David J$$b62
000155333 7001_ $$aCharlesworth, Gavin$$b63
000155333 7001_ $$aChen, Honglei$$b64
000155333 7001_ $$aChinnery, Patrick F$$b65
000155333 7001_ $$aChong, Sean$$b66
000155333 7001_ $$aClarke, Carl E$$b67
000155333 7001_ $$aCookson, Mark R$$b68
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