FDA perspectives on potential microarray-based clinical diagnostics

by Težak, Živana, Ranamukhaarachchi, Daya, Russek-Cohen, Estelle, Gutman, Steven I
Published 2006

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

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

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

by 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
Published 2012-06-01

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

by 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
Published 2012

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

by 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
Published in Patterns (N Y) (2021)

Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes

by 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
Published in Nat Biotechnol (2019)

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

by 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.
Published 2013

A Roadmap for Regulatory Science Research for Next Generation Sequencing Informatics

by 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
Published in Sci Transl Med (2016)

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

by 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.
Published in J Mol Diagn (2017)