Whole-Genome Sequencing of Two Canine Herpesvirus 1 (CaHV-1) Isolates and Clinicopathological Outcomes of Infection in French Bulldog Puppies by Angela Maria Rocchigiani, Loris Bertoldi, Elisabetta Coradduzza, Giada Lostia, Davide Pintus, Rosario Scivoli, Maria Giovanna Cancedda, Mariangela Stefania Fiori, Roberto Bechere, Anna Pina Murtino, Giovanni Pala, Giusy Cardeti, Simona Macioccu, Maria Antonietta Dettori, Antonio Pintore, Ciriaco Ligios, Giantonella Puggioni

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Hypothyroidism and rheumatoid arthritis: a two-sample Mendelian randomization study by Yang Gao, Zheng-Rui Fan, Fang-Yuan Shi, Fang-Yuan Shi

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Rare copy number variant analysis in case–control studies using snp array data: a scalable and automated data analysis pipeline by Haydee Artaza, Ksenia Lavrichenko, Anette S. B. Wolff, Ellen C. Røyrvik, Marc Vaudel, Stefan Johansson

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A structure-based in silico analysis of the Kell blood group system by Gabriele Mayr, Maike Bublitz, Tim A. Steiert, Britt-Sabina Löscher, Michael Wittig, Hesham ElAbd, Christoph Gassner, Christoph Gassner, Andre Franke

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Multidimensional Analytical Study of Heart Sounds: A Review by Akash Kumar Bhoi, Karma Sonam Sherpa, Bidita Khandelwal

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Knowledge-driven binning approach for rare variant association analysis: application to neuroimaging biomarkers in Alzheimer’s disease by Dokyoon Kim, Anna O. Basile, Lisa Bang, Emrin Horgusluoglu, Seunggeun Lee, Marylyn D. Ritchie, Andrew J. Saykin, Kwangsik Nho

Subjects: “…Rare variant analysis…”
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Genomic data of two Greek Vitis varieties by George Tsiolas, Sofia Michailidou, Antiopi Tsoureki, Anagnostis Argiriou

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Rare coding variants in RCN3 are associated with blood pressure by Karen Y. He, Tanika N. Kelly, Heming Wang, Jingjing Liang, Luke Zhu, Brian E. Cade, Themistocles L. Assimes, Lewis C. Becker, Amber L. Beitelshees, Lawrence F. Bielak, Adam P. Bress, Jennifer A. Brody, Yen-Pei Christy Chang, Yi-Cheng Chang, Paul S. de Vries, Ravindranath Duggirala, Ervin R. Fox, Nora Franceschini, Anna L. Furniss, Yan Gao, Xiuqing Guo, Jeffrey Haessler, Yi-Jen Hung, Shih-Jen Hwang, Marguerite Ryan Irvin, Rita R. Kalyani, Ching-Ti Liu, Chunyu Liu, Lisa Warsinger Martin, May E. Montasser, Paul M. Muntner, Stanford Mwasongwe, Take Naseri, Walter Palmas, Muagututi’a Sefuiva Reupena, Kenneth M. Rice, Wayne H.-H. Sheu, Daichi Shimbo, Jennifer A. Smith, Beverly M. Snively, Lisa R. Yanek, Wei Zhao, John Blangero, Eric Boerwinkle, Yii-Der Ida Chen, Adolfo Correa, L. Adrienne Cupples, Joanne E. Curran, Myriam Fornage, Jiang He, Lifang Hou, Robert C. Kaplan, Sharon L. R. Kardia, Eimear E. Kenny, Charles Kooperberg, Donald Lloyd-Jones, Ruth J. F. Loos, Rasika A. Mathias, Stephen T. McGarvey, Braxton D. Mitchell, Kari E. North, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, D. C. Rao, Susan Redline, Alex P. Reiner, Stephen S. Rich, Jerome I. Rotter, Kent D. Taylor, Russell Tracy, Ramachandran S. Vasan, The Samoan Obesity, Lifestyle and Genetic Adaptations Study (OLaGA) Group, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Alanna C. Morrison, Daniel Levy, Aravinda Chakravarti, Donna K. Arnett, Xiaofeng Zhu

Subjects: “…Rare variant analysis…”
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Gene-based multiple regression association testing for combined examination of common and low frequency variants in quantitative trait analysis by Yun Joo eYoo, Yun Joo eYoo, Lei eSun, Lei eSun, Shelley B. Bull, Shelley B. Bull

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Meta-Qtest: meta-analysis of quadratic test for rare variants by Jieun Ka, Jaehoon Lee, Yongkang Kim, Bermseok Oh, T2D-GENES Consortium, Taesung Park

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Multi-Allelic Mitochondrial DNA Deletions in an Adult Dog with Chronic Weakness, Exercise Intolerance and Lactic Acidemia by G. Diane Shelton, James R. Mickelson, Steven G. Friedenberg, Jonah N. Cullen, Jaya M. Mehra, Ling T. Guo, Katie M. Minor

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Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population by Robert W. Read, Karen A. Schlauch, Vincent C. Lombardi, Elizabeth T. Cirulli, Nicole L. Washington, James T. Lu, Joseph J. Grzymski, Joseph J. Grzymski

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Use of hemagglutinin and neuraminidase amplicon-based high-throughput sequencing with variant analysis to detect co-infection and resolve identical consensus sequences of seasonal... by Temitope O. C. Faleye, Deborah Adams, Sangeet Adhikari, Helen Sandrolini, Rolf U. Halden, Arvind Varsani, Matthew Scotch

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Challenging popular tools for the annotation of genetic variations with a real case, pathogenic mutations of lysosomal alpha-galactosidase by Chiara Cimmaruta, Valentina Citro, Giuseppina Andreotti, Ludovica Liguori, Maria Vittoria Cubellis, Bruno Hay Mele

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OVAS: an open-source variant analysis suite with inheritance modelling by Monika Mozere, Mehmet Tekman, Jameela Kari, Detlef Bockenhauer, Robert Kleta, Horia Stanescu

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Integrated approach to generate artificial samples with low tumor fraction for somatic variant calling benchmarking by Aldo Sergi, Luca Beltrame, Sergio Marchini, Marco Masseroli

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Effects of Holding Temperature on Bainite Transformation in Cr-Mo Steel by M. Sarizam, Y. Komizo

Subjects: “…Variant analysis…”
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An Initial Survey of the Performances of Exome Variant Analysis and Clinical Reporting Among Diagnostic Laboratories in China by Kuo Zhang, Kuo Zhang, Guigao Lin, Dongsheng Han, Dongsheng Han, Yanxi Han, Jian Wang, Yiping Shen, Yiping Shen, Yiping Shen, Jinming Li

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Characterising power quality disturbances resulting from current limiting fuse operation by N. Ortiz S., J. Blanco S., G. Ordoñez P., V. Barrera N.

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Germline variant analysis from a cohort of patients with severe hypertriglyceridemia in Brazil by Camila Mendes, Thereza Loureiro, Darine Villela, Marcelo Imbroinise Bittencourt, Joselito Sobreira, Diana Bermeo, Mireille Gomes, Dayse Alencar, Luciana Santos Serrao de Castro, Rodrigo Ambrosio Fock, Maria Luisa Tinoco, Henrique Galvão, Cristovam Scapulatempo-Neto, Katia Schiavetti, Andreza A. Senerchia, Maria Helane Costa Gurgel

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