FDA perspectives on potential microarray-based clinical diagnostics

Tekijä Težak, Živana, Ranamukhaarachchi, Daya, Russek-Cohen, Estelle, Gutman, Steven I
Julkaistu 2006

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

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

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

Tekijä 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
Julkaistu 2012-06-01

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

Tekijä 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
Julkaistu 2012

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

Tekijä 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
Julkaisussa Patterns (N Y) (2021)

Best Practices for Benchmarking Germline Small Variant Calls in Human Genomes

Tekijä 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
Julkaisussa Nat Biotechnol (2019)

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

Tekijä 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.
Julkaistu 2013

A Roadmap for Regulatory Science Research for Next Generation Sequencing Informatics

Tekijä 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
Julkaisussa Sci Transl Med (2016)

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

Tekijä 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.
Julkaisussa J Mol Diagn (2017)