FDA perspectives on potential microarray-based clinical diagnostics

per Težak, Živana, Ranamukhaarachchi, Daya, Russek-Cohen, Estelle, Gutman, Steven I
Publicat 2006

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

per Boja, Emily, Težak, Živana, Zhang, Bing, Wang, Pei, Johanson, Elaine, Hinton, Denise, Rodriguez, Henry
Publicat a Nat Med (2018)

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

per 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
Publicat 2012-06-01

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

per 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
Publicat 2012

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

per 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
Publicat a Patterns (N Y) (2021)

Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes

per 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
Publicat a Nat Biotechnol (2019)

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

per 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.
Publicat 2013

A Roadmap for Regulatory Science Research for Next Generation Sequencing Informatics

per 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
Publicat a Sci Transl Med (2016)

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

per 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.
Publicat a J Mol Diagn (2017)