FDA perspectives on potential microarray-based clinical diagnostics

por Težak, Živana, Ranamukhaarachchi, Daya, Russek-Cohen, Estelle, Gutman, Steven I
Publicado 2006

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

por Boja, Emily, Težak, Živana, Zhang, Bing, Wang, Pei, Johanson, Elaine, Hinton, Denise, Rodriguez, Henry
Publicado en Nat Med (2018)

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

por 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
Publicado 2012-06-01

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

por 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
Publicado 2012

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

por 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
Publicado en Patterns (N Y) (2021)

Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes

por 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
Publicado en Nat Biotechnol (2019)

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

por 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.
Publicado 2013

A Roadmap for Regulatory Science Research for Next Generation Sequencing Informatics

por 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
Publicado en Sci Transl Med (2016)

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

por 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.
Publicado en J Mol Diagn (2017)