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Androniki Menelaou

Showing results (1-10 of 11) with videos related to

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Bioinformatics (Oxford, England)|October 25, 2012
Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffoldAndroniki Menelaou, Jonathan Marchini
Genes|April 8, 2014
Association claims in the sequencing eraSara L Pulit, Maarten Leusink, Androniki Menelaou, et al.
Nature Genetics|May 19, 2015
Genome-wide patterns and properties of de novo mutations in humansLaurent C Francioli, Paz P Polak, Amnon Koren, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Cell Reports|December 16, 2014
Genomic and functional overlap between somatic and germline chromosomal rearrangementsSebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, et al.
Nature Communications|January 23, 2015
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility lociRegina C Betz, Lynn Petukhova, Stephan Ripke, et al.
Plos Genetics|February 6, 2014
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysmsMitja I Kurki, Emília Ilona Gaál, Johannes Kettunen, et al.
European Journal of Human Genetics : EJHG|May 30, 2013
The Genome of the Netherlands: design, and project goalsDorret I Boomsma, Cisca Wijmenga, Eline P Slagboom, et al.
Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|October 25, 2012
Genotype calling and phasing using next-generation sequencing reads and a haplotype scaffoldAndroniki Menelaou, Jonathan Marchini
Genes|April 8, 2014
Association claims in the sequencing eraSara L Pulit, Maarten Leusink, Androniki Menelaou, et al.
Nature Genetics|May 19, 2015
Genome-wide patterns and properties of de novo mutations in humansLaurent C Francioli, Paz P Polak, Amnon Koren, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Improved imputation quality of low-frequency and rare variants in European samples using the 'Genome of The Netherlands'Patrick Deelen, Androniki Menelaou, Elisabeth M van Leeuwen, et al.
Cell Reports|December 16, 2014
Genomic and functional overlap between somatic and germline chromosomal rearrangementsSebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, et al.
Nature Communications|January 23, 2015
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility lociRegina C Betz, Lynn Petukhova, Stephan Ripke, et al.
Plos Genetics|February 6, 2014
High risk population isolate reveals low frequency variants predisposing to intracranial aneurysmsMitja I Kurki, Emília Ilona Gaál, Johannes Kettunen, et al.
European Journal of Human Genetics : EJHG|May 30, 2013
The Genome of the Netherlands: design, and project goalsDorret I Boomsma, Cisca Wijmenga, Eline P Slagboom, et al.
Nature|October 4, 2015
An integrated map of structural variation in 2,504 human genomesPeter H Sudmant, Tobias Rausch, Eugene J Gardner, et al.
Nature Communications|March 10, 2015
Genome of The Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levelsElisabeth M van Leeuwen, Lennart C Karssen, Joris Deelen, et al.
Pageof 2