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      Deep learning enables genetic analysis of the human thoracic aorta

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      1 , 2 , 3 , 4 , 5 , 3 , 4 , 2 , 6 , 4 , 7 , 8 , 9 , 3 , 5 , 1 , 2 , 3 , 7 , 3 , 10 , 3 , 4 , 3 , 3 , 4 , 7 , 11 , 3 , 3 , 12 , 8 , 13 , 14 , 3 , 15 , 4 , 5 , 16 , 5 , 17 , 8 , 13 , 14 , 1 , 2 , 5 , 18 , 19 , 1 , 2 , 3 , 5 , 7 , 20 , 1 , 2 , 3 , 5 , 21 , 1 , 2 , 3 , 4 , 5 , *
      Nature genetics

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          Abstract

          Enlargement or aneurysm of the aorta predisposes to dissection, an important cause of sudden death. We trained a deep learning model to evaluate the dimensions of the ascending and descending thoracic aorta in 4.6 million cardiac magnetic resonance images from the UK Biobank. We then conducted genome-wide association studies in 39,688 individuals, identifying 82 loci associated with ascending and 47 with descending thoracic aortic diameter, of which 14 loci overlapped. Transcriptome-wide analyses, rare-variant burden tests, and human aortic single nucleus RNA sequencing prioritized genes including SVIL, which was strongly associated with descending aortic diameter. A polygenic score for ascending aortic diameter was associated with thoracic aortic aneurysm in 385,621 UK Biobank participants (HR = 1.43 per s.d.; CI 1.32-1.54; P = 3.3 × 10 −20). Our results illustrate the potential for rapidly defining quantitative traits with deep learning, an approach that can be broadly applied to biomedical images.

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          Deep Residual Learning for Image Recognition

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            Is Open Access

            The mutational constraint spectrum quantified from variation in 141,456 humans

            Genetic variants that inactivate protein-coding genes are a powerful source of information about the phenotypic consequences of gene disruption: genes that are crucial for the function of an organism will be depleted of such variants in natural populations, whereas non-essential genes will tolerate their accumulation. However, predicted loss-of-function variants are enriched for annotation errors, and tend to be found at extremely low frequencies, so their analysis requires careful variant annotation and very large sample sizes 1 . Here we describe the aggregation of 125,748 exomes and 15,708 genomes from human sequencing studies into the Genome Aggregation Database (gnomAD). We identify 443,769 high-confidence predicted loss-of-function variants in this cohort after filtering for artefacts caused by sequencing and annotation errors. Using an improved model of human mutation rates, we classify human protein-coding genes along a spectrum that represents tolerance to inactivation, validate this classification using data from model organisms and engineered human cells, and show that it can be used to improve the power of gene discovery for both common and rare diseases.
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              ImageNet classification with deep convolutional neural networks

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                Author and article information

                Journal
                9216904
                2419
                Nat Genet
                Nat Genet
                Nature genetics
                1061-4036
                1546-1718
                10 October 2021
                January 2022
                26 November 2021
                26 May 2022
                : 54
                : 1
                : 40-51
                Affiliations
                [1 ]Division of Cardiology, Massachusetts General Hospital, Boston, Massachusetts, USA
                [2 ]Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA
                [3 ]Cardiovascular Disease Initiative, Broad Institute, Cambridge, Massachusetts, USA
                [4 ]Precision Cardiology Laboratory, The Broad Institute & Bayer US LLC, Cambridge, Massachusetts, USA
                [5 ]Harvard Medical School, Boston, Massachusetts, USA
                [6 ]Division of Vascular and Endovascular Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA
                [7 ]Data Sciences Platform, Broad Institute, Cambridge, Massachusetts, USA
                [8 ]Framingham Heart Study, Boston University and National Heart, Lung, and Blood Institute, Framingham, Massachusetts, USA
                [9 ]Department of Medicine, Section of Computational Biomedicine, Boston University School of Medicine, Boston, Massachusetts, USA
                [10 ]Department of Medicine, Center for Genomic Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA
                [11 ]Masonic Medical Research Institute, Utica, New York, USA
                [12 ]University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
                [13 ]Department of Medicine, Cardiology and Preventive Medicine Sections, Boston University School of Medicine, Boston, Massachusetts, USA
                [14 ]Epidemiology Department, Boston University School of Public Health, Boston, Massachusetts, USA
                [15 ]Department of Medicine, Divisions of Cardiovascular Medicine and Genetics, Brigham and Women’s Hospital, Boston, Massachusetts, USA
                [16 ]Cancer Center, Massachusetts General Hospital, Boston, Massachusetts, USA
                [17 ]Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts, USA
                [18 ]Department of Radiology, Harvard Medical School, Boston, Massachusetts, USA
                [19 ]Cardiovascular Imaging Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA
                [20 ]GV, Mountain View, California, USA
                [21 ]Thoracic Aortic Center, Massachusetts General Hospital, Boston, Massachusetts, USA
                Author notes

                Author Contributions

                J.P.P. and P.T.E. conceived of the study. J.P.P. and M.N. annotated images. J.P.P., M.D.C., S.J.F., S.N.F., S.H.C., H.L., E.L.C. and M.N. conducted bioinformatic analyses. E.L.C., A.A., A.-D.A., N.R.T., D.J., and J.R.S. contributed to the rapid autopsy human aorta analysis. H.L., R.S.V., E.J.B., and U.H. contributed to the GWAS replication. J.P.P., M.E.L., and P.T.E. wrote the paper. S.K., A.G.B., L.-C.W., P.B., A.W.H., C.R., S.K.V., R.M.G., C.M.S., J.E.H., S.A.L., and A.A.P. contributed to the analysis plan or provided critical revisions.

                Article
                NIHMS1745044
                10.1038/s41588-021-00962-4
                8758523
                34837083
                148c0ea0-508d-4efc-be91-d0cae5f4d284

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                Genetics
                Genetics

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