FDA perspectives on potential microarray-based clinical diagnostics

von Težak, Živana, Ranamukhaarachchi, Daya, Russek-Cohen, Estelle, Gutman, Steven I
Veröffentlicht 2006

Right data for right patient—a precisionFDA NCI–CPTAC Multi-omics Mislabeling Challenge

von Boja, Emily, Težak, Živana, Zhang, Bing, Wang, Pei, Johanson, Elaine, Hinton, Denise, Rodriguez, Henry
Veröffentlicht in Nat Med (2018)

Characterization of whole genome amplified (WGA) DNA for use in genotyping assay development

von Han Tao, Chang Ching-Wei, Kwekel Joshua C, Chen Ying, Ge Yun, Martinez-Murillo Francisco, Roscoe Donna, Težak Živana, Philip Reena, Bijwaard Karen, Fuscoe James C
Veröffentlicht 2012-06-01

Characterization of whole genome amplified (WGA) DNA for use in genotyping assay development

von Han, Tao, Chang, Ching-Wei, Kwekel, Joshua C, Chen, Ying, Ge, Yun, Martinez-Murillo, Francisco, Roscoe, Donna, Težak, Živana, Philip, Reena, Bijwaard, Karen, Fuscoe, James C
Veröffentlicht 2012

A community effort to identify and correct mislabeled samples in proteogenomic studies

von Yoo, Seungyeul, Shi, Zhiao, Wen, Bo, Kho, SoonJye, Pan, Renke, Feng, Hanying, Chen, Hong, Carlsson, Anders, Edén, Patrik, Ma, Weiping, Raymer, Michael, Maier, Ezekiel J., Tezak, Zivana, Johanson, Elaine, Hinton, Denise, Rodriguez, Henry, Zhu, Jun, Boja, Emily, Wang, Pei, Zhang, Bing
Veröffentlicht in Patterns (N Y) (2021)

Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes

von Krusche, Peter, Trigg, Len, Boutros, Paul C., Mason, Christopher E., De La Vega, Francisco M., Moore, Benjamin L., Gonzalez-Porta, Mar, Eberle, Michael A., Tezak, Zivana, Lababidi, Samir, Truty, Rebecca, Asimenos, George, Funke, Birgit, Fleharty, Mark, Chapman, Brad A., Salit, Marc, Zook, Justin M
Veröffentlicht in Nat Biotechnol (2019)

Statistical Design for Biospecimen Cohort Size in Proteomics-based Biomarker Discovery and Verification Studies

von Skates, Steven J., Gillette, Michael A., LaBaer, Joshua, Carr, Steven A., Anderson, N. Leigh, Liebler, Daniel C., Ransohoff, David, Rifai, Nader, Kondratovich, Marina, Težak, Živana, Mansfield, Elizabeth, Oberg, Ann L., Wright, Ian, Barnes, Grady, Gail, Mitchell, Mesri, Mehdi, Kinsinger, Christopher R., Rodriguez, Henry, Boja, Emily S.
Veröffentlicht 2013

A Roadmap for Regulatory Science Research for Next Generation Sequencing Informatics

von Altman, Russ B, Prabhu, Snehit, Sidow, Arend, Zook, Justin, Goldfeder, Rachel, Litwack, David, Ashley, Euan, Asimenos, George, Bustamante, Carlos, Donigan, Katherine, Giacomini, Kathy, Johansen, Elaine, Khuri, Natalia, Lee, Eunice, Liang, Sharon, Linden, Carol, Salit, Marc, Serang, Omar, Tezak, Zivana, Wall, Dennis, Mansfield, Elizabeth, Kass-Hout, Taha
Veröffentlicht in Sci Transl Med (2016)

Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings

von Lubin, Ira M., Aziz, Nazneen, Babb, Lawrence J., Ballinger, Dennis, Bisht, Himani, Church, Deanna M., Cordes, Shaun, Eilbeck, Karen, Hyland, Fiona, Kalman, Lisa, Landrum, Melissa, Lockhart, Edward R., Maglott, Donna, Marth, Gabor, Pfeifer, John D., Rehm, Heidi L., Roy, Somak, Tezak, Zivana, Truty, Rebecca, Ullman-Cullere, Mollie, Voelkerding, Karl V., Worthey, Elizabeth A., Zaranek, Alexander W., Zook, Justin M.
Veröffentlicht in J Mol Diagn (2017)