Whole Exome Analysis to Analyse the Mutational Profiles of Taiwanese Patients with Breast Cancer
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Publisher
Springer Nature Switzerland
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-52385-4_24
Reference28 articles.
1. Guo, Y., et al.: Comparative study of exome copy number variation estimation tools using array comparative genomic hybridization as control. Biomed. Res. Int. 2013, 915636 (2013). https://doi.org/10.1155/2013/915636
2. Stephens, P.J., et al.: The landscape of cancer genes and mutational processes in breast cancer. Nature 486(7403), 400–404 (2012). https://doi.org/10.1038/nature11017
3. Cobain, E.F., Milliron, K.J., Merajver, S.D.: Updates on breast cancer genetics: Clinical implications of detecting syndromes of inherited increased susceptibility to breast cancer. Semin. Oncol. 43(5), 528–535 (2016). https://doi.org/10.1053/j.seminoncol.2016.10.001
4. Noh, J.M., Kim, J., Cho, D.Y., Choi, D.H., Park, W., Huh, S.J.: Exome sequencing in a breast cancer family without BRCA mutation. Radiation Oncol. J. 33(2), 149 (2015). https://doi.org/10.3857/roj.2015.33.2.149
5. Goh, G., Choi, M.: Application of whole exome sequencing to identify disease-causing variants in inherited human diseases. Genom. Inform 10(4), 214–219 (2012). https://doi.org/10.5808/GI.2012.10.4.214
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