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Articles, 2 records found
Articles 2 records found  
1.
5 p, 359.4 KB lme4qtl : Linear mixed models with flexible covariance structure for genetic studies of related individuals / Ziyatdinov, Andrey (Chan School of Public Health) ; Vázquez-Santiago, Miquel (Hospital de la Santa Creu i Sant Pau (Barcelona, Catalunya)) ; Brunel, Helena (Hospital de la Santa Creu i Sant Pau (Barcelona, Catalunya)) ; Martinez-Perez, Angel (Institut d'Investigació Biomèdica Sant Pau) ; Aschard, Hugues (Biostatistique et Biologie Intégrative (C3BI)) ; Soria Fernández, José Manuel (Institut d'Investigació Biomèdica Sant Pau) ; Universitat Autònoma de Barcelona
Quantitative trait locus (QTL) mapping in genetic data often involves analysis of correlated observations, which need to be accounted for to avoid false association signals. This is commonly performed by modeling such correlations as random effects in linear mixed models (LMMs). [...]
2018 - 10.1186/s12859-018-2057-x
BMC bioinformatics, Vol. 19 Núm. 1 (27 2018) , p. 68  
Detailed record - Creative Commons
2.
15 p, 1.1 MB Next generation sequencing to dissect the genetic architecture of KNG1 and F11 loci using factor XI levels as an intermediate phenotype of thrombosis / Martin-Fernandez, Laura (Institut d'Investigació Biomèdica Sant Pau) ; Gavidia-Bovadilla, Giovana (Universitat Politècnica de Catalunya) ; Corrales Insa, Irene (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; Brunel, Helena (Institut d'Investigació Biomèdica Sant Pau) ; Ramírez, Lorena (Hospital Universitari Vall d'Hebron. Institut de Recerca) ; López, Sonia (Institut d'Investigació Biomèdica Sant Pau) ; Souto, Juan Carlos (Institut d'Investigació Biomèdica Sant Pau) ; Vidal, Francisco (Centro de Investigación Biomédica en Red en Enfermedades Cardiovasculares) ; Soria Fernández, José Manuel (Institut d'Investigació Biomèdica Sant Pau) ; Universitat Autònoma de Barcelona
Venous thromboembolism is a complex disease with a high heritability. There are significant associations among Factor XI (FXI) levels and SNPs in the KNG1 and F11 loci. Our aim was to identify the genetic variation of KNG1 and F11 that might account for the variability of FXI levels. [...]
2017 - 10.1371/journal.pone.0176301
PloS one, Vol. 12 (april 2017)  
Detailed record - Creative Commons

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