P188: Synchronized long-read genome, methylene, epigenome, and transcriptome for a putative small fiber peripheral polyneuropathy research study von Glanz, Max, Gonzaludo, Nina, Tseng, Elizabeth, Merritt, Matthew, Wang, Eric

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Correction: Estimating the burden and economic impact of pediatric genetic disease von Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.

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P600: pb-StarPhase: A phase-aware pharmacogenomic diplotyper for long-read sequencing data von Holt, James, Harting, John, Gonzaludo, Nina, Kronenberg, Zev, Saunders, Christopher, Eberle, Michael

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The diagnostic trajectory of infants and children with clinical features of genetic disease von Schroeder, Brock E., Gonzaludo, Nina, Everson, Katie, Than, Kyi-Sin, Sullivan, Jeff, Taft, Ryan J., Belmont, John W.

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P478: Simultaneous analysis of 50+ different repeat expansions with twist target enrichment and PacBio HiFi sequencing von Han, Tina, Corbitt, Holly, Dolzhenko, Egor, Gonzaludo, Nina, Kingan, Sarah, Tung, Po-Yuan, Toro, Esteban, Locklear, Chad

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P472: Highly scalable pharmacogenomic panel testing with hybrid capture and long-read sequencing von Gonzaludo, Nina, Kingan, Sarah, Harting, John, Baybayan, Primo, Zhang, Siyuan, Han, Tina, Arbiza, Leonardo, Yang, Yao, Hammond, Nathan, Scott, Stuart

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Identification of a kinase profile that predicts chromosome damage induced by small molecule kinase inhibitors von Olaharski, Andrew J, Gonzaludo, Nina, Bitter, Hans, Goldstein, David, Kirchner, Stephan, Uppal, Hirdesh, Kolaja, Kyle

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eP138: An informatics star allele calling workflow for direct typing of CYP2D6 from fully phased variants using PacBio HiFi reads von Harting, John, Kronenberg, Zev, Gonzaludo, Nina

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A meta-analysis of QTL for diabetes-related traits in rodents von Schmidt, Christian, Gonzaludo, Nina P, Strunk, Sarah, Dahm, Stefan, Schuchhardt, Johannes, Kleinjung, Frank, Wuschke, Stefan, Joost, Hans-Georg, Al-Hasani, Hadi

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Estimating the burden and economic impact of pediatric genetic disease von Gonzaludo, Nina, Belmont, John W., Gainullin, Vladimir G., Taft, Ryan J.

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Three patients with homozygous familial hypercholesterolemia: Genomic sequencing and kindred analysis von Wong, Karen H.Y., Levy‐Sakin, Michal, Ma, Walfred, Gonzaludo, Nina, Mak, Angel C.Y., Vaka, Dedeepya, Poon, Annie, Chu, Catherine, Lao, Richard, Balamir, Melek, Grenville, Zoe, Wong, Nicolas, Kane, John P., Kwok, Pui‐Yan, Malloy, Mary J., Pullinger, Clive R.

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Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data von Chen, Xiao, Shen, Fei, Gonzaludo, Nina, Malhotra, Alka, Rogert, Cande, Taft, Ryan J., Bentley, David R., Eberle, Michael A.

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An efficient genotyper and star-allele caller for pharmacogenomics von Hari, Ananth, Zhou, Qinghui, Gonzaludo, Nina, Harting, John, Scott, Stuart A, Qin, Xiang, Scherer, Steve, Sahinalp, S Cenk, Numanagić, Ibrahim

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Cost-effectiveness of genome sequencing for diagnosing patients with undiagnosed rare genetic diseases von Incerti, Devin, Xu, Xiang-Ming, Chou, Jacquelyn W., Gonzaludo, Nina, Belmont, John W., Schroeder, Brock E.

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An efficient genotyper and star-allele caller for pharmacogenomics von Hari, Ananth, Zhou, Qinghui, Gonzaludo, Nina, Harting, John, Scott, Stuart A, Qin, Xiang, Scherer, Steve, Sahinalp, S Cenk, Numanagić, Ibrahim

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CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project von Gaedigk, Andrea, Boone, Erin C, Scherer, Steven E, Lee, Seung-Been, Numanagić, Ibrahim, Sahinalp, Cenk, Smith, Joshua D, McGee, Sean, Radhakrishnan, Aparna, Qin, Xiang, Wang, Wendy Y, Farrow, Emily G, Gonzaludo, Nina, Halpern, Aaron L, Nickerson, Deborah A, Miller, Neil A, Pratt, Victoria M, Kalman, Lisa V

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Publisher Correction: Cyrius: accurate CYP2D6 genotyping using whole-genome sequencing data von Chen, Xiao, Shen, Fei, Gonzaludo, Nina, Malhotra, Alka, Rogert, Cande, Taft, Ryan J., Bentley, David R., Eberle, Michael A.

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PARC report: a health-systems focus on reimbursement and patient access to pharmacogenomics testing von L Rogers, Sara, Keeling, Nicholas J, Giri, Jyothsna, Gonzaludo, Nina, Jones, J Shawn, Glogowski, Emily, Formea, Christine M

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CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis von Gaedigk, Andrea, Boone, Erin C., Scherer, Steven E., Lee, Seung-been, Numanagić, Ibrahim, Sahinalp, Cenk, Smith, Joshua D., McGee, Sean, Radhakrishnan, Aparna, Qin, Xiang, Wang, Wendy Y., Farrow, Emily G., Gonzaludo, Nina, Halpern, Aaron L., Nickerson, Deborah A., Miller, Neil A., Pratt, Victoria M., Kalman, Lisa V.

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HGV2012: Leveraging Next-Generation Technology and Large Datasets to Advance Disease Research von Gonzaludo, Nina, Zheng, Hong-Xiang, Wang, Jiucun, Chanock, Stephen J., Jin, Li, Scherer, Stephen, Wijmenga, Cisca, Kwok, Pui-Yan, Brookes, Anthony J.

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