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Shallow whole genome sequencing on circulating cell-free DNA allows reliable noninvasive copy-number profiling in neuroblastoma patients

(2017) CLINICAL CANCER RESEARCH . 23(20). p.6305-6314
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MYCN AMPLIFICATION, ACTIONABLE MUTATIONS, LIQUID BIOPSIES, ARRAY-CGH, N-MYC, THERAPY, CANCER, BLOOD, HETEROGENEITY, HYBRIDIZATION

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Chicago
Van Roy, Nadine, Malaïka Van Der Linden, Björn Menten, Annelies Dheedene, Charlotte Vandeputte, Jo Van Dorpe, Genevieve Laureys, et al. 2017. “Shallow Whole Genome Sequencing on Circulating Cell-free DNA Allows Reliable Noninvasive Copy-number Profiling in Neuroblastoma Patients.” Clinical Cancer Research 23 (20): 6305–6314.
APA
Van Roy, N., Van Der Linden, M., Menten, B., Dheedene, A., Vandeputte, C., Van Dorpe, J., Laureys, G., et al. (2017). Shallow whole genome sequencing on circulating cell-free DNA allows reliable noninvasive copy-number profiling in neuroblastoma patients. CLINICAL CANCER RESEARCH , 23(20), 6305–6314.
Vancouver
1.
Van Roy N, Van Der Linden M, Menten B, Dheedene A, Vandeputte C, Van Dorpe J, et al. Shallow whole genome sequencing on circulating cell-free DNA allows reliable noninvasive copy-number profiling in neuroblastoma patients. CLINICAL CANCER RESEARCH . 2017;23(20):6305–14.
MLA
Van Roy, Nadine, Malaïka Van Der Linden, Björn Menten, et al. “Shallow Whole Genome Sequencing on Circulating Cell-free DNA Allows Reliable Noninvasive Copy-number Profiling in Neuroblastoma Patients.” CLINICAL CANCER RESEARCH 23.20 (2017): 6305–6314. Print.
@article{8551633,
  author       = {Van Roy, Nadine and Van Der Linden, Mala{\"i}ka and Menten, Bj{\"o}rn and Dheedene, Annelies and Vandeputte, Charlotte and Van Dorpe, Jo and Laureys, Genevieve and Renard, Marleen and Sante, Tom and Lammens, Tim and De Wilde, Bram and Speleman, Franki and De Preter, Katleen},
  issn         = {1078-0432},
  journal      = {CLINICAL CANCER RESEARCH },
  keyword      = {MYCN AMPLIFICATION,ACTIONABLE MUTATIONS,LIQUID BIOPSIES,ARRAY-CGH,N-MYC,THERAPY,CANCER,BLOOD,HETEROGENEITY,HYBRIDIZATION},
  language     = {eng},
  number       = {20},
  pages        = {6305--6314},
  title        = {Shallow whole genome sequencing on circulating cell-free DNA allows reliable noninvasive copy-number profiling in neuroblastoma patients},
  url          = {http://dx.doi.org/10.1158/1078-0432.ccr-17-0675},
  volume       = {23},
  year         = {2017},
}

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