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Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data.

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Introduction to Statistical Methods of Analysis (Geography)

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ToppGene Suite for gene list enrichment analysis and candidate gene prioritization. Nucleic Acids Res. Improved human disease candidate gene prioritization using mouse phenotype. BMC Bioinforma. DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants.

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Lek, M. Analysis of protein-coding genetic variation in 60, humans.

Scan Statistics: Methods and Applications (Statistics for Industry and Technology)

Short, P. De novo mutations in regulatory elements in neurodevelopmental disorders. Ascano, M. Download references. We are grateful to all of the families at the participating Simons Simplex Collection SSC sites, as well as the principal investigators A. Beaudet, R. Bernier, J. Constantino, E.

Cook, E. Fombonne, D. Geschwind, R. Goin-Kochel, E. Hanson, D. Grice, A. Klin, D. Ledbetter, C. Lord, C. Martin, D. Martin, R. Maxim, J.

Scan Statistics - Methods and Applications | Joseph Glaz | Springer

Miles, O. Ousley, K. Pelphrey, B. Peterson, J. Piggot, C. Saulnier, M. State, W. Stone, J. Sutcliffe, C. Walsh, Z. Warren, E. We thank Laura Scott for helpful comments. Correspondence to Iuliana Ionita-Laza. Peer review information: Nature Communications thanks the anonymous reviewer s for their contribution to the peer review of this work.

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