Хайлтын үр дүнгүүд - Venner, Eric

Evolutionary Trace Annotation of Protein Function in the Structural Proteome -н Erdin, Serkan, Ward, R. Matthew, Venner, Eric, Lichtarge, Olivier

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Function prediction from networks of local evolutionary similarity in protein structure -н Erdin, Serkan, Venner, Eric, Lisewski, Andreas Martin, Lichtarge, Olivier

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ETAscape: analyzing protein networks to predict enzymatic function and substrates in Cytoscape -н Bachman, Benjamin J., Venner, Eric, Lua, Rhonald C., Erdin, Serkan, Lichtarge, Olivier

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Accurate Protein Structure Annotation through Competitive Diffusion of Enzymatic Functions over a Network of Local Evolutionary Similarities -н Venner, Eric, Lisewski, Andreas Martin, Erdin, Serkan, Ward, R. Matthew, Amin, Shivas R., Lichtarge, Olivier

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

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Evolutionary Trace Annotation Server: automated enzyme function prediction in protein structures using 3D templates -н Matthew Ward, R., Venner, Eric, Daines, Bryce, Murray, Stephen, Erdin, Serkan, Kristensen, David M., Lichtarge, Olivier

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ARBoR: an identity and security solution for clinical reporting -н Venner, Eric, Murugan, Mullai, Hale, Walker, Jones, Jordan M, Lu, Shan, Yi, Victoria, Gibbs, Richard A

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Accounting for epistatic interactions improves the functional analysis of protein structures -н Wilkins, Angela D., Venner, Eric, Marciano, David C., Erdin, Serkan, Atri, Benu, Lua, Rhonald C., Lichtarge, Olivier

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Genome sequencing analysis of a family with a child displaying severe abdominal distention and recurrent hypoglycemia -н Liu, Jidong, Ding, Guolian, Zou, Kexin, Jiang, Ziru, Zhang, Junyu, Lu, Yunhua, Pignata, Antonella, Venner, Eric, Liu, Pengfei, Liu, Zhandong, Wangler, Michael F., Sun, Zheng

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Artificial Intelligence and Cardiovascular Genetics -н Krittanawong, Chayakrit, Johnson, Kipp W., Choi, Edward, Kaplin, Scott, Venner, Eric, Murugan, Mullai, Wang, Zhen, Glicksberg, Benjamin S., Amos, Christopher I., Schatz, Michael C., Tang, W. H. Wilson

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Harmonizing variant classification for return of results in the All of Us Research Program -н Harrison, Steven M., Austin‐Tse, Christina A., Kim, Serra, Lebo, Matthew, Leon, Annette, Murdock, David, Radhakrishnan, Aparna, Shirts, Brian H., Steeves, Marcie, Venner, Eric, Gibbs, Richard A., Jarvik, Gail P., Rehm, Heidi L.

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Exome variant discrepancies due to reference-genome differences -н Li, He, Dawood, Moez, Khayat, Michael M., Farek, Jesse R., Jhangiani, Shalini N., Khan, Ziad M., Mitani, Tadahiro, Coban-Akdemir, Zeynep, Lupski, James R., Venner, Eric, Posey, Jennifer E., Sabo, Aniko, Gibbs, Richard A.

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Neptune: An environment for the delivery of genomic medicine -н Venner, Eric, Yi, Victoria, Murdock, David, Kalla, Sara E., Wu, Tsung-Jung, Sabo, Aniko, Li, Shoudong, Meng, Qingchang, Tian, Xia, Murugan, Mullai, Cohen, Michelle, Kovar, Christie, Wei, Wei-Qi, Chung, Wendy K., Weng, Chunhua, Wiesner, Georgia L., Jarvik, Gail P., Muzny, Donna, Gibbs, Richard A.

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Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients with Left Ventricular Non-Compaction -н Miszalski-Jamka, Karol, Jefferies, John L., Mazur, Wojciech, Głowacki, Jan, Hu, Jianhong, Lazar, Monika, Gibbs, Richard A., Liczko, Jacek, Kłyś, Jan, Venner, Eric, Muzny, Donna M., Rycaj, Jarosław, Białkowski, Jacek, Kluczewska, Ewa, Kalarus, Zbigniew, Jhangiani, Shalini, Al-Khalidi, Hussein, Kukulski, Tomasz, Lupski, James R., Craigen, William J., Bainbridge, Matthew N.

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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 -н 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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Best practices for the interpretation and reporting of clinical whole genome sequencing -н Austin-Tse, Christina A., Jobanputra, Vaidehi, Perry, Denise L., Bick, David, Taft, Ryan J., Venner, Eric, Gibbs, Richard A., Young, Ted, Barnett, Sarah, Belmont, John W., Boczek, Nicole, Chowdhury, Shimul, Ellsworth, Katarzyna A., Guha, Saurav, Kulkarni, Shashikant, Marcou, Cherisse, Meng, Linyan, Murdock, David R., Rehman, Atteeq U., Spiteri, Elizabeth, Thomas-Wilson, Amanda, Kearney, Hutton M., Rehm, Heidi L.

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Empowering genomic medicine by establishing critical sequencing result data flows: the eMERGE example -н Aronson, Samuel, Babb, Lawrence, Ames, Darren, Gibbs, Richard A, Venner, Eric, Connelly, John J, Marsolo, Keith, Weng, Chunhua, Williams, Marc S, Hartzler, Andrea L, Liang, Wayne H, Ralston, James D, Devine, Emily Beth, Murphy, Shawn, Chute, Christopher G, Caraballo, Pedro J, Kullo, Iftikhar J, Freimuth, Robert R, Rasmussen, Luke V, Wehbe, Firas H, Peterson, Josh F, Robinson, Jamie R, Wiley, Ken, Overby Taylor, Casey

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The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results -н Kullo, Iftikhar J., Olson, Janet, Fan, Xiao, Jose, Merin, Safarova, Maya, Breitkopf, Carmen Radecki, Winkler, Erin, Kochan, David C., Snipes, Sara, Pacyna, Joel E., Carney, Meaghan, Chute, Christopher G., Gupta, Jyoti, Jose, Sheethal, Venner, Eric, Murugan, Mullai, Jiang, Yunyun, Zordok, Magdi, Farwati, Medhat, Philogene, Maraisha, Smith, Erica, Shaibi, Gabriel Q., Caraballo, Pedro, Freimuth, Robert, Lindor, Noralane M., Sharp, Richard, Thibodeau, Stephen N.

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Genomic considerations for FHIR®; eMERGE implementation lessons -н Murugan, Mullai, Babb, Lawrence J., Taylor, Casey Overby, Rasmussen, Luke V., Freimuth, Robert R., Venner, Eric, Yan, Fei, Yi, Victoria, Granite, Stephen J., Zouk, Hana, Aronson, Samuel J., Power, Kevin, Fedotov, Alex, Crosslin, David R., Fasel, David, Jarvik, Gail P., Hakonarson, Hakon, Bangash, Hana, Kullo, Iftikhar J., Connolly, John J., Nestor, Jordan G., Caraballo, Pedro J., Wei, WeiQi, Wiley, Ken, Rehm, Heidi L., Gibbs, Richard A.

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Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel -н Chiang, Theodore, Liu, Xiuping, Wu, Tsung-Jung, Hu, Jianhong, Sedlazeck, Fritz J., White, Simon, Schaid, Daniel, Andrade, Mariza de, Jarvik, Gail P., Crosslin, David, Stanaway, Ian, Carrell, David S., Connolly, John J., Hakonarson, Hakon, Groopman, Emily E., Gharavi, Ali G., Fedotov, Alexander, Bi, Weimin, Leduc, Magalie S., Murdock, David R., Jiang, Yunyun, Meng, Linyan, Eng, Christine M., Wen, Shu, Yang, Yaping, Muzny, Donna M., Boerwinkle, Eric, Salerno, William, Venner, Eric, Gibbs, Richard A.

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