المؤلفون: Zaboli, Ghazal, Ameur, Adam, Igl, Wilmar, Johansson, Åsa, Hayward, Caroline, Vitart, Veronique, Campbell, Susan, Zgaga, Lina, Polasek, Ozren, Schmitz, Gerd, van Duijn, Cornelia, Oostra, Ben, Pramstaller, Peter, Hicks, Andrew, Meitinger, Tomas, Rudan, Igor, Wright, Alan, Wilson, James F., Campbell, Harry, Gyllensten, Ulf

المصدر: European Journal of Human Genetics. 20(1):77-83

مصطلحات موضوعية: pooling, next-generation DNA sequencing, SOLiD, SNP, indels

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-167177

المؤلفون: Tomas Meitinger, Veronique Vitart, Andrew A. Hicks, Alan F. Wright, Cornelia M. van Duijn, Ghazal Zaboli, Åsa Johansson, Ozren Polasek, Caroline Hayward, Wilmar Igl, James F. Wilson, Adam Ameur, Ben A. Oostra, Ulf Gyllensten, Harry Campbell, Peter P. Pramstaller, Igor Rudan, Gerd Schmitz, Lina Zgaga, Susan Campbell

المساهمون: Epidemiology, Clinical Genetics

المصدر: European Journal of Human Genetics
Zaboli, G, Ameur, A, Igl, W, Johansson, Å, Hayward, C, Vitart, V, Campbell, S, Zgaga, L, Polasek, O, Schmitz, G, van Duijn, C, Oostra, B, Pramstaller, P, Hicks, A, Meitinger, T, Rudan, I, Wright, A, Wilson, J F & Campbell, H & Gyllensten, U 2012, ' Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits ', European Journal of Human Genetics, vol. 20, no. 1, pp. 77-83 . https://doi.org/10.1038/ejhg.2011.138
European Journal of Human Genetics; Vol 20
European Journal of Human Genetics, 20(1), 77-83. Nature Publishing Group
Eur. J. Hum. Genet. 20, 77-83 (2012)

مصطلحات موضوعية: sequencing, pool, genomics, Genotype, Quantitative Trait Loci, Glucose Transport Proteins, Facilitative, Single-nucleotide polymorphism, Biology, Quantitative trait locus, Polymorphism, Single Nucleotide, Sensitivity and Specificity, Article, DNA sequencing, Deep sequencing, Cohort Studies, 03 medical and health sciences, Gene Frequency, INDEL Mutation, pooling, next-generation DNA sequencing, SOLiD, SNP, indels, Genetics, Chromosomes, Human, Humans, Genetic Testing, Genotyping, Genetics (clinical), Exome sequencing, 030304 developmental biology, 0303 health sciences, Genome, Human, 030305 genetics & heredity, Computational Biology, Lipase, Sequence Analysis, DNA, SNP genotyping, Genomic Structural Variation, Human genome, Sequence Alignment

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec12da54a0e1cd689ff0cbab910495c5
https://hdl.handle.net/1765/37208