Performance Characterization and Validation of Saliva as an Alternative Specimen Source for Detecting Hereditary Breast Cancer Mutations by Next Generation Sequencing

por Meghnani, Varsha, Mohammed, Nadeem, Giauque, Christopher, Nahire, Rahul, David, Thomas
Publicado 2016

Universal Germline Testing of Unselected Cancer Patients Detects Pathogenic Variants Missed by Standard Guidelines without Increasing Healthcare Costs

por Perkins, Adrienne T., Haslem, Derrick, Goldsberry, Jessica, Shortt, Katherine, Sittig, Laura, Raghunath, Sharanya, Giauque, Christopher, Snow, Shawnee, Fulde, Gail, Moulton, Bryce, Jones, David, Nadauld, Lincoln
Publicado 2021

The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health

por Walton, Nephi A., Hafen, Brent, Graceffo, Sara, Sutherland, Nykole, Emmerson, Melanie, Palmquist, Rachel, Formea, Christine M., Purcell, Maricel, Heale, Bret, Brown, Matthew A., Danford, Christopher J., Rachamadugu, Sumathi I., Person, Thomas N., Shortt, Katherine A., Christensen, G. Bryce, Evans, Jared M., Raghunath, Sharanya, Johnson, Christopher P., Knight, Stacey, Le, Viet T., Anderson, Jeffrey L., Van Meter, Margaret, Reading, Teresa, Haslem, Derrick S., Hansen, Ivy C., Batcher, Betsey, Barker, Tyler, Sheffield, Travis J., Yandava, Bhaskara, Taylor, David P., Ranade-Kharkar, Pallavi, Giauque, Christopher C., Eyring, Kenneth R., Breinholt, Jesse W., Miller, Mickey R., Carter, Payton R., Gillman, Jason L., Gunn, Andrew W., Knowlton, Kirk U., Bonkowsky, Joshua L., Stefansson, Kari, Nadauld, Lincoln D., McLeod, Howard L.
Publicado 2022