MYC Copy Number Detection in Clinical Samples Using a Digital DNA-Hybridization and Detection Method
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Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-1476-1_18
Reference11 articles.
1. Beroukhim R, Mermel CH, Porter D et al (2010) The landscape of somatic copy-number alteration across human cancers. Nature 463(7283):899–905. https://doi.org/10.1038/nature08822
2. Gilbert MTP, Haselkorn T, Bunce M et al (2007) The isolation of nucleic acids from fixed, paraffin-embedded tissues—which methods are useful when? PLoS One 2(6):e537. https://doi.org/10.1371/journal.pone.0000537
3. Mehrotra M, Luthra R, Abraham R et al (2017) Validation of quantitative PCR-based assays for detection of gene copy number aberrations in formalin-fixed, paraffin embedded solid tumor samples. Cancer Genet 212–213:24–31. https://doi.org/10.1016/j.cancergen.2017.03.002
4. Kallioniemi A, Visakorpi T, Karhu R et al (1996) Gene copy number analysis by fluorescence in situ hybridization and comparative genomic hybridization. Methods 9:113–121. https://doi.org/10.1006/meth.1996.0015
5. Kader T, Goode DL, Wong SQ et al (2016) Copy number analysis by low coverage whole genome sequencing using ultra low-input DNA from formalin-fixed paraffin embedded tumor tissue. Genome Med 8(1):121. https://doi.org/10.1186/s13073-016-0375-z
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