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Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.

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Title: Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.
Authors: Bocher O; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Institute of Translational Genomics, Helmholtz Zentrum München, Munich, Germany., Ludwig TE; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; CHU Brest, Brest, France., Oglobinsky MS; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France., Marenne G; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France., Deleuze JF; Centre National de Recherche en Génomique Humaine CNRGH, Institut de Biologie François Jacob, Université Paris Saclay, CEA, Evry, France., Suryakant S; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, team ELEANOR, UMR 1219, Bordeaux, France., Odeberg J; Science for Life Laboratory, Department of Protein Science, CBH, KTH Royal Institute of Technology, Stockholm, Sweden.; Department of Clinical Medicine, Faculty of Health Science, The Arctic University of Tromsö, Tromsö, Norway., Morange PE; Aix Marseille Univ, INSERM, INRAE, C2VN, Marseille, France., Trégouët DA; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, team ELEANOR, UMR 1219, Bordeaux, France., Perdry H; CESP Inserm, U1018, UFR Médecine, Univ Paris-Sud, Université Paris-Saclay, Villejuif, France., Génin E; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; CHU Brest, Brest, France.
Source: PLoS genetics [PLoS Genet] 2022 Sep 16; Vol. 18 (9), pp. e1009923. Date of Electronic Publication: 2022 Sep 16 (Print Publication: 2022).
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Testing for association with rare variants in the coding and non-coding genome: RAVA-FIRST, a new approach based on CADD deleteriousness score.
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  Data: <searchLink fieldCode="AU" term="%22Bocher+O%22">Bocher O</searchLink>; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; Institute of Translational Genomics, Helmholtz Zentrum München, Munich, Germany.<br /><searchLink fieldCode="AU" term="%22Ludwig+TE%22">Ludwig TE</searchLink>; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; CHU Brest, Brest, France.<br /><searchLink fieldCode="AU" term="%22Oglobinsky+MS%22">Oglobinsky MS</searchLink>; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.<br /><searchLink fieldCode="AU" term="%22Marenne+G%22">Marenne G</searchLink>; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.<br /><searchLink fieldCode="AU" term="%22Deleuze+JF%22">Deleuze JF</searchLink>; Centre National de Recherche en Génomique Humaine CNRGH, Institut de Biologie François Jacob, Université Paris Saclay, CEA, Evry, France.<br /><searchLink fieldCode="AU" term="%22Suryakant+S%22">Suryakant S</searchLink>; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, team ELEANOR, UMR 1219, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Odeberg+J%22">Odeberg J</searchLink>; Science for Life Laboratory, Department of Protein Science, CBH, KTH Royal Institute of Technology, Stockholm, Sweden.; Department of Clinical Medicine, Faculty of Health Science, The Arctic University of Tromsö, Tromsö, Norway.<br /><searchLink fieldCode="AU" term="%22Morange+PE%22">Morange PE</searchLink>; Aix Marseille Univ, INSERM, INRAE, C2VN, Marseille, France.<br /><searchLink fieldCode="AU" term="%22Trégouët+DA%22">Trégouët DA</searchLink>; University of Bordeaux, Inserm, Bordeaux Population Health Research Center, team ELEANOR, UMR 1219, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Perdry+H%22">Perdry H</searchLink>; CESP Inserm, U1018, UFR Médecine, Univ Paris-Sud, Université Paris-Saclay, Villejuif, France.<br /><searchLink fieldCode="AU" term="%22Génin+E%22">Génin E</searchLink>; Univ Brest, Inserm, EFS, UMR 1078, GGB, Brest, France.; CHU Brest, Brest, France.
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  Data: <searchLink fieldCode="JN" term="%22101239074%22">PLoS genetics</searchLink> [PLoS Genet] 2022 Sep 16; Vol. 18 (9), pp. e1009923. <i>Date of Electronic Publication: </i>2022 Sep 16 (<i>Print Publication: </i>2022).
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