Genomics

Displaying 1 - 18 of 18CSV
Stear, B. J., Mohseni Ahooyi, T., Simmons, J. A., Kollar, C., Hartman, L., Beigel, K., Lahiri, A., Vasisht, S., Callahan, T. J., Nemarich, C. M., Silverstein, J. C., & Taylor, D. M. (2024). Petagraph: A large-scale unifying knowledge graph framework for integrating biomolecular and biomedical data. Scientific Data, 11(1). https://doi.org/10.1038/s41597-024-04070-w
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Ramos, M. A., Bonini, K. E., Scarimbolo, L., Kelly, N. R., Insel, B., Suckiel, S. A., Brown, K., Di Biase, M., Gallagher, K. M., Lopez, J., Aguiñiga, K. L., Marathe, P. N., Maria, E., Odgis, J. A., Rodriguez, J. E., Rodriguez, M. A., Ruiz, N., Sebastin, M., Yelton, N. M., … Horowitz, C. R. (2024). Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research. The American Journal of Human Genetics, 111(12), 2607–2617. https://doi.org/10.1016/j.ajhg.2024.10.015
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Jakaria Al-Mujahidy, Sk. Md., Kryukov, K., Ikeo, K., Saito, K., Uddin, Md. E., & Ibn Sina, A. A. (2024). Functional genomic analysis of the isolated potential probiotic Lactobacillus delbrueckii subsp. indicus TY-11 and its comparison with other Lactobacillus delbrueckii strains. Microbiology Spectrum, 12(7). https://doi.org/10.1128/spectrum.03470-23
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Li, Y., Ye, J., Huang, Y., Wu, J., Liu, X., Ahmed, S., & Osterman, T. (2024). Minimal Common Oncology Data Elements Genomics Pilot Project: Enhancing Oncology Research Through Electronic Health Record Interoperability at Vanderbilt University Medical Center. JCO Clinical Cancer Informatics, 8. https://doi.org/10.1200/cci.23.00249
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Madden, E. B., Hindorff, L. A., Bonham, V. L., Akintobi, T. H., Burchard, E. G., Baker, K. E., Begay, R. L., Carpten, J. D., Cox, N. J., Di Francesco, V., Dillard, D. A., Fletcher, F. E., Fullerton, S. M., Garrison, N. A., Hammack-Aviran, C. M., Hiratsuka, V. Y., Hildreth, J. E. K., Horowitz, C. R., Hughes Halbert, C. A., … Green, E. D. (2024). Advancing genomics to improve health equity. Nature Genetics, 56(5), 752–757. https://doi.org/10.1038/s41588-024-01711-z
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Zhong, G., Choi, Y. A., & Shen, Y. (2023). VBASS enables integration of single cell gene expression data in Bayesian association analysis of rare variants. Communications Biology, 6(1). https://doi.org/10.1038/s42003-023-05155-9
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Clayton, E. W., Smith, M. E., Anderson, K. C., Chung, W. K., Connolly, J. J., Fullerton, S. M., McGowan, M. L., Peterson, J. F., Prows, C. A., Sabatello, M., & Holm, I. A. (2023). Studying the impact of translational genomic research: Lessons from eMERGE. The American Journal of Human Genetics, 110(7), 1021–1033. https://doi.org/10.1016/j.ajhg.2023.05.011
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Linder, J. E., Allworth, A., Bland, H. T., Caraballo, P. J., Chisholm, R. L., Clayton, E. W., Crosslin, D. R., Dikilitas, O., DiVietro, A., Esplin, E. D., Forman, S., Freimuth, R. R., Gordon, A. S., Green, R., Harden, M. V., Holm, I. A., Jarvik, G. P., Karlson, E. W., Labrecque, S., … Peterson, J. F. (2023). Returning integrated genomic risk and clinical recommendations: The eMERGE study. Genetics in Medicine, 25(4), 100006. https://doi.org/10.1016/j.gim.2023.100006
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Iqbal, M. A., Broeckel, U., Levy, B., Skinner, S., Sahajpal, N. S., Rodriguez, V., Stence, A., Awayda, K., Scharer, G., Skinner, C., Stevenson, R., Bossler, A., Nagy, P. L., & Kolhe, R. (2023). Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases. The Journal of Molecular Diagnostics, 25(3), 175–188. https://doi.org/10.1016/j.jmoldx.2022.12.005
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Wang, Y., Fan, J. L., Melms, J. C., Amin, A. D., Georgis, Y., Barrera, I., Ho, P., Tagore, S., Abril-Rodríguez, G., He, S., Jin, Y., Biermann, J., Hofree, M., Caprio, L., Berhe, S., Khan, S. A., Henick, B. S., Ribas, A., Macosko, E. Z., … Izar, B. (2023). Multimodal single-cell and whole-genome sequencing of small, frozen clinical specimens. Nature Genetics, 55(1), 19–25. https://doi.org/10.1038/s41588-022-01268-9
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Yang, K., Cao, Y., Gurjao, C., Liu, Y., Guo, C.-G., Lo, C.-H., Zong, X., Drew, D., Geraghty, C., Prezioso, E., Moore, M., Williams, C., Riley, T., Saul, M., Ogino, S., Giannakis, M., Bass, A., Schoen, R. E., & Chan, A. T. (2022). Clinical and Genomic Characterization of Interval Colorectal Cancer in 3 Prospective Cohorts. Gastroenterology, 163(6), 1522-1530.e5. https://doi.org/10.1053/j.gastro.2022.08.020
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Sherafati, A., Elsekaily, O., Saadatagah, S., Kochan, D. C., Lee, C., Wiesner, G. L., Liu, C., Dellefave-Castillo, L., Namjou, B., Perez, E. F., Salvati, Z. M., Connolly, J. J., Hakonarson, H., Williams, M. S., Jarvik, G. P., Chung, W. K., McNally, E. M., Manolio, T. A., & Kullo, I. J. (2022). Pathogenic variants in arteriopathy genes detected in a targeted sequencing study: Penetrance and 1-year outcomes after return of results. Genetics in Medicine, 24(10), 2123–2133. https://doi.org/10.1016/j.gim.2022.07.007
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Lemke, A. A., Esplin, E. D., Goldenberg, A. J., Gonzaga-Jauregui, C., Hanchard, N. A., Harris-Wai, J., Ideozu, J. E., Isasi, R., Landstrom, A. P., Prince, A. E. R., Turbitt, E., Sabatello, M., Schrier Vergano, S. A., Taylor, M. R. G., Yu, J.-H., Brothers, K. B., & Garrison, N. A. (2022). Addressing underrepresentation in genomics research through community engagement. The American Journal of Human Genetics, 109(9), 1563–1571. https://doi.org/10.1016/j.ajhg.2022.08.005
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Hayeck, T. J., Stong, N., Baugh, E., Dhindsa, R., Turner, T. N., Malakar, A., Mosbruger, T. L., Shaw, G. T.-W., Duan, Y., Ionita-Laza, I., Goldstein, D., & Allen, A. S. (2022). Ancestry adjustment improves genome-wide estimates of regional intolerance. Genetics. https://doi.org/10.1093/genetics/iyac050
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Walker, A. (2022). Diversity, Profit, Control: An Empirical Study of Industry Employees’ Views on Ethics in Private Sector Genomics. AJOB Empirical Bioethics, 13(3), 166–178. https://doi.org/10.1080/23294515.2022.2063993
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