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Abstract
The diagnostic yield of exome and genome sequencing remains low (8–70%), due to incomplete knowledge on the genes that cause disease. To improve this, we use RNA-seq data from 31,499 samples to predict which genes cause specific disease phenotypes, and develop GeneNetwork Assisted Diagnostic Optimization (GADO). We show that this unbiased method, which does not rely upon specific knowledge on individual genes, is effective in both identifying previously unknown disease gene associations, and flagging genes that have previously been incorrectly implicated in disease. GADO can be run on www.genenetwork.nl by supplying HPO-terms and a list of genes that contain candidate variants. Finally, applying GADO to a cohort of 61 patients for whom exome-sequencing analysis had not resulted in a genetic diagnosis, yields likely causative genes for ten cases.
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Details
; Sipko van Dam 2 ; Herkert, Johanna C 2
; Karjalainen, Juha M 2 ; Brugge, Harm 2 ; Abbott, Kristin M 2
; van Diemen, Cleo C 2 ; Paul A van der Zwaag 2 ; Gerkes, Erica H 2 ; Zonneveld-Huijssoon, Evelien 2
; Boer-Bergsma, Jelkje J 2 ; Folkertsma, Pytrik 2 ; Gillett, Tessa 2 ; K Joeri van der Velde 1 ; Roan Kanninga 1 ; Peter C van den Akker 2 ; Jan, Sabrina Z 2 ; Hoorntje, Edgar T 3 ; te Rijdt, Wouter P 3
; Vos, Yvonne J 2 ; Jongbloed, Jan D H 2 ; Conny M A van Ravenswaaij-Arts 2 ; Sinke, Richard 2 ; Sikkema-Raddatz, Birgit 2 ; Kerstjens-Frederikse, Wilhelmina S 2
; Swertz, Morris A 1
; Franke, Lude 2
1 University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands; University of Groningen, University Medical Center Groningen, Genomics Coordination Center, Groningen, The Netherlands
2 University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands
3 University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands; Netherlands Heart Institute, Utrecht, The Netherlands




