Truvari: refined structural variant comparison preserves allelic diversity von English, Adam C, Menon, Vipin K, Gibbs, Richard A, Metcalf, Ginger A, Sedlazeck, Fritz J

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The gut mycobiome of the Human Microbiome Project healthy cohort von Nash, Andrea K, Auchtung, Thomas A, Wong, Matthew C, Smith, Daniel P, Gesell, Jonathan R, Ross, Matthew C, Stewart, Christopher J, Metcalf, Ginger A, Muzny, Donna M, Gibbs, Richard A, Ajami, Nadim J, Petrosino, Joseph F

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Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program von Venner, Eric, Muzny, Donna, Smith, Joshua D, Walker, Kimberly, Neben, Cynthia L, Lockwood, Christina M, Empey, Phillip E, Metcalf, Ginger A, Kachulis, Chris, Mian, Sana, Musick, Anjene, Rehm, Heidi L, Harrison, Steven, Gabriel, Stacey, Gibbs, Richard A, Nickerson, Deborah, Zhou, Alicia Y, Doheny, Kimberly, Ozenberger, Bradley, Topper, Scott E, Lennon, Niall J

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Whole-genome sequencing study of serum peptide levels: the Atherosclerosis Risk in Communities study von de Vries, Paul S, Yu, Bing, Feofanova, Elena V, Metcalf, Ginger A, Brown, Michael R, Zeighami, Atefeh L, Liu, Xiaoming, Muzny, Donna M, Gibbs, Richard A, Boerwinkle, Eric, Morrison, Alanna C

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Sequence-Based Analysis of Lipid-Related Metabolites in a Multiethnic Study von Feofanova, Elena V, Yu, Bing, Metcalf, Ginger A, Liu, Xiaoming, Muzny, Donna, Below, Jennifer E, Wagenknecht, Lynne E, Gibbs, Richard A, Morrison, Alanna C, Boerwinkle, Eric

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Identification of allele-specific KIV-2 repeats and impact on Lp(a) measurements for cardiovascular disease risk von Behera, Sairam, Belyeu, Jonathan R, Chen, Xiao, Paulin, Luis F, Nguyen, Ngoc Quynh H, Newman, Emma, Mahmoud, Medhat, Menon, Vipin K, Qi, Qibin, Joshi, Parag, Marcovina, Santica, Rossi, Massimiliano, Roller, Eric, Han, James, Onuchic, Vitor, Avery, Christy L, Ballantyne, Christie M, Rodriguez, Carlos J, Kaplan, Robert C, Muzny, Donna M, Metcalf, Ginger A, Gibbs, Richard A, Yu, Bing, Boerwinkle, Eric, Eberle, Michael A, Sedlazeck, Fritz J

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Temporal development of the gut microbiome in early childhood from the TEDDY study von Stewart, Christopher J., Ajami, Nadim J., O’Brien, Jacqueline L., Hutchinson, Diane S., Smith, Daniel P., Wong, Matthew C., Ross, Matthew C., Lloyd, Richard E., Doddapaneni, HarshaVardhan, Metcalf, Ginger A., Muzny, Donna, Gibbs, Richard A., Vatanen, Tommi, Huttenhower, Curtis, Xavier, Ramnik J., Rewers, Marian, Hagopian, William, Toppari, Jorma, Ziegler, Anette-G., She, Jin-Xiong, Akolkar, Beena, Lernmark, Ake, Hyoty, Heikki, Vehik, Kendra, Krischer, Jeffrey P., Petrosino, Joseph F.

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Loss-of-function variants influence the human serum metabolome von Yu, Bing, Li, Alexander H, Metcalf, Ginger A, Muzny, Donna M, Morrison, Alanna C, White, Simon, Mosley, Thomas H, Gibbs, Richard A, Boerwinkle, Eric

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Patient and Clinician Perceptions of Precision Cardiology Care: Findings From the HeartCare Study von Smith, Hadley Stevens, Sanchez, Clarissa E., Maag, Ronald, Buentello, Alexandria, Murdock, David R., Metcalf, Ginger A., Hadley, Trevor D., Riconda, Daniel L., Boerwinkle, Eric, Wehrens, Xander H.T., Ballantyne, Christie M., Gibbs, Richard A., McGuire, Amy L., Pereira, Stacey

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Unveiling microbial diversity: harnessing long-read sequencing technology von Agustinho, Daniel P., Fu, Yilei, Menon, Vipin K., Metcalf, Ginger A., Treangen, Todd J., Sedlazeck, Fritz J.

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Structure and function of the healthy pre-adolescent pediatric gut microbiome von Hollister, Emily B, Riehle, Kevin, Luna, Ruth Ann, Weidler, Erica M, Rubio-Gonzales, Michelle, Mistretta, Toni-Ann, Raza, Sabeen, Doddapaneni, Harsha V, Metcalf, Ginger A, Muzny, Donna M, Gibbs, Richard A, Petrosino, Joseph F, Shulman, Robert J, Versalovic, James

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Leveraging Human Microbiome Features to Diagnose and Stratify Children with Irritable Bowel Syndrome von Hollister, Emily B., Oezguen, Numan, Chumpitazi, Bruno P., Luna, Ruth Ann, Weidler, Erica M., Rubio-Gonzales, Michelle, Dahdouli, Mahmoud, Cope, Julia L., Mistretta, Toni-Ann, Raza, Sabeen, Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Petrosino, Joseph F., Heitkemper, Margaret, Savidge, Tor C., Shulman, Robert J., Versalovic, James

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Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors von Pankratz, Nathan, Wei, Peng, Brody, Jennifer A, Chen, Ming-Huei, de Vries, Paul S, Huffman, Jennifer E, Stimson, Mary Rachel, Auer, Paul L, Boerwinkle, Eric, Cushman, Mary, de Maat, Moniek P M, Folsom, Aaron R, Franco, Oscar H, Gibbs, Richard A, Haagenson, Kelly K, Hofman, Albert, Johnsen, Jill M, Kovar, Christie L, Kraaij, Robert, McKnight, Barbara, Metcalf, Ginger A, Muzny, Donna, Psaty, Bruce M, Tang, Weihong, Uitterlinden, André G, van Rooij, Jeroen G J, Dehghan, Abbas, O'Donnell, Christopher J, Reiner, Alex P, Morrison, Alanna C, Smith, Nicholas L

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Whole genome sequence analysis of serum amino acid levels von Yu, Bing, de Vries, Paul S, Metcalf, Ginger A, Wang, Zhe, Feofanova, Elena V, Liu, Xiaoming, Muzny, Donna Marie, Wagenknecht, Lynne E, Gibbs, Richard A, Morrison, Alanna C, Boerwinkle, Eric

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Inter and intra-host diversity of RSV in hematopoietic stem cell transplant adults with normal and delayed viral clearance von Avadhanula, Vasanthi, Agustinho, Daniel Paiva, Menon, Vipin Kumar, Chemaly, Roy F, Shah, Dimpy P, Qin, Xiang, Surathu, Anil, Doddapaneni, Harshavardhan, Muzny, Donna M, Metcalf, Ginger A, Cregeen, Sara Javornik, Gibbs, Richard A, Petrosino, Joseph F, Sedlazeck, Fritz J, Piedra, Pedro A

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Fully resolved assembly of Cryptosporidium parvum von Menon, Vipin K, Okhuysen, Pablo C, Chappell, Cynthia L, Mahmoud, Medhat, Mahmoud, Medhat, Meng, Qingchang, Doddapaneni, Harsha, Vee, Vanesa, Han, Yi, Salvi, Sejal, Bhamidipati, Sravya, Kottapalli, Kavya, Weissenberger, George, Shen, Hua, Ross, Matthew C, Hoffman, Kristi L, Cregeen, Sara Javornik, Muzny, Donna M, Metcalf, Ginger A, Gibbs, Richard A, Petrosino, Joseph F, Sedlazeck, Fritz J

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The Implementation Science for Genomic Health Translation (INSIGHT) Study in Epilepsy: Protocol for a Learning Health Care System von Feofanova, Elena Valeryevna, Zhang, Guo-Qiang, Lhatoo, Samden, Metcalf, Ginger A, Boerwinkle, Eric, Venner, Eric

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Rare Genetic Variants Associated With Sudden Cardiac Arrest in the Young: A Prospective, Population-Based Study von Holmstrom, Lauri, Chaudhary, Ninad S., Nakamura, Kotoka, Chugh, Harpriya, Uy-Evanado, Audrey, Norby, Faye, Metcalf, Ginger A., Menon, Vipin K., Yu, Bing, Boerwinkle, Eric, Chugh, Sumeet S., Akdemir, Zeynep, Kransdorf, Evan P.

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Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation von Eicher, John D., Chen, Ming-Huei, Pitsillides, Achilleas N., Lin, Honghuang, Veeraraghavan, Narayanan, Brody, Jennifer A., Metcalf, Ginger A., Muzny, Donna M., Gibbs, Richard A., Becker, Diane M., Becker, Lewis C., Faraday, Nauder, Mathias, Rasika A., Yanek, Lisa R., Boerwinkle, Eric, Adrienne Cupples, L., Johnson, Andrew D.

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Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk von Yu, Bing, Pulit, Sara L, Hwang, Shih-Jen, Brody, Jennifer A, Amin, Najaf, Auer, Paul L, Bis, Joshua C, Boerwinkle, Eric, Burke, Gregory L, Chakravarti, Aravinda, Correa, Adolfo, Dreisbach, Albert W, Franco, Oscar H, Ehret, Georg B, Franceschini, Nora, Hofman, Albert, Lin, Dan-Yu, Metcalf, Ginger A, Musani, Solomon K, Muzny, Donna, Palmas, Walter, Raffel, Leslie, Reiner, Alex, Rice, Ken, Rotter, Jerome I, Veeraraghavan, Narayanan, Fox, Ervin, Guo, Xiuqing, North, Kari E, Gibbs, Richard A, van Duijn, Cornelia M, Psaty, Bruce M, Levy, Daniel, Newton-Cheh, Christopher, Morrison, Alanna C

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