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Rennert H, Eng K, Zhang T, et al. Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care. NPJ Genom Med. 2016;1doi: 10.1038/npjgenmed.2016.19.
Rennert, H., Eng, K., Zhang, T., Tan, A., Xiang, J., Romanel, A., Kim, R., Tam, W., Liu, Y. C., Bhinder, B., Cyrta, J., Beltran, H., Robinson, B., Mosquera, J. M., Fernandes, H., Demichelis, F., Sboner, A., Kluk, M., Rubin, M. A., & Elemento, O. (2016). Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care. NPJ genomic medicine, 1. https://doi.org/10.1038/npjgenmed.2016.19
Rennert, Hanna, et al. "Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care." NPJ genomic medicine vol. 1 (2016). doi: https://doi.org/10.1038/npjgenmed.2016.19
Rennert H, Eng K, Zhang T, Tan A, Xiang J, Romanel A, Kim R, Tam W, Liu YC, Bhinder B, Cyrta J, Beltran H, Robinson B, Mosquera JM, Fernandes H, Demichelis F, Sboner A, Kluk M, Rubin MA, Elemento O. Development and validation of a whole-exome sequencing test for simultaneous detection of point mutations, indels and copy-number alterations for precision cancer care. NPJ Genom Med. 2016;1. doi: 10.1038/npjgenmed.2016.19. Epub 2016 Jul 20. PMID: 28781886; PMCID: PMC5539963.
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