Cargando…

Detection of copy number alterations in cell-free tumor DNA from plasma

BACKGROUND: Somatic copy number alterations (SCNAs) occurring in tumors can provide information about tumor classification, patient's outcome or treatment targets. Liquid biopsies, incl. plasma samples containing circulating cell-free tumor DNA (ccfDNA) can be used to assess SCNAs for clinical...

Descripción completa

Detalles Bibliográficos
Autores principales:	Østrup, Olga, Ahlborn, Lise Barlebo, Lassen, Ulrik, Mau-Sørensen, Morten, Nielsen, Finn Cilius
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2017
Materias:	Regular Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390666/ https://www.ncbi.nlm.nih.gov/pubmed/28417079 http://dx.doi.org/10.1016/j.bbacli.2017.03.006

Ejemplares similares

Plasma total cell-free DNA is a prognostic biomarker of overall survival in metastatic solid tumour patients
por: Viller Tuxen, Ida, et al.
Publicado: (2019)

Cell-free DNA in newly diagnosed patients with glioblastoma – a clinical prospective feasibility study
por: Nørøxe, Dorte Schou, et al.
Publicado: (2019)

Circulating tumor DNA as a marker of treatment response in BRAF V600E mutated non-melanoma solid tumors
por: Ahlborn, Lise Barlebo, et al.
Publicado: (2018)

Application of cell-free DNA for genomic tumor profiling: a feasibility study
por: Ahlborn, Lise B., et al.
Publicado: (2019)

Actionable Molecular Alterations Are Revealed in Majority of Advanced Non-Small Cell Lung Cancer Patients by Genomic Tumor Profiling at Progression after First Line Treatment
por: Frank, Malene Støchkel, et al.
Publicado: (2021)

Neoepitope load, T cell signatures and PD-L2 as combined biomarker strategy for response to checkpoint inhibition immunotherapy
por: Borch, Annie, et al.
Publicado: (2023)

Tumor mutational burden and purity adjustment before and after treatment with temozolomide in 27 paired samples of glioblastoma: a prospective study
por: Schou Nørøxe, Dorte, et al.
Publicado: (2021)

Alterations in telomere length and mitochondrial DNA copy number in human lymphocytes on short-term exposure to moderate hypoxia
por: Alam, Mohammad Rizwan, et al.
Publicado: (2020)

High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer
por: Bertelsen, Birgitte, et al.
Publicado: (2019)

Massively parallel sequencing of cell-free DNA in plasma for detecting gynaecological tumour-associated copy number alteration
por: Nakabayashi, Makoto, et al.
Publicado: (2018)

A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data
por: Gabrielaite, Migle, et al.
Publicado: (2021)

Resistance of Leishmania infantum to allopurinol is associated with chromosome and gene copy number variations including decrease in the S-adenosylmethionine synthetase (METK) gene copy number
por: Yasur-Landau, Daniel, et al.
Publicado: (2018)

Cell‐free DNA copy number variations in plasma from colorectal cancer patients
por: Li, Jian, et al.
Publicado: (2017)

Contribution of copy number variations to the risk of severe eating disorders
por: Kushima, Itaru, et al.
Publicado: (2022)

Establishment of tumor-specific copy number alterations from plasma DNA of patients with cancer
por: Heitzer, Ellen, et al.
Publicado: (2013)

Publisher Correction: Massively parallel sequencing of cell-free DNA in plasma for detecting gynaecological tumour-associated copy number alteration
por: Nakabayashi, Makoto, et al.
Publicado: (2018)

Detection of circulating tumor-derived material in peripheral blood of pediatric sarcoma patients: A systematic review
por: Kjær, Eva Kristine Ruud, et al.
Publicado: (2023)

Polygenic risk scores in schizophrenia with clinically significant copy number variants
por: Taniguchi, Satoru, et al.
Publicado: (2019)

Cell-free DNA chromosome copy number variations predict outcomes in plasma cell myeloma
por: Qiang, Wanting, et al.
Publicado: (2023)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

Alteration in plasma free amino acid levels and its association with gout
por: Mahbub, MH, et al.
Publicado: (2017)

Maternal versus paternal inheritance of a 132 bp 11p15.5 microdeletion affecting KCNQ1OT1 and associated phenotypes
por: Stoltze, Ulrik Kristoffer, et al.
Publicado: (2023)

Increasing chromosome 1 copy number parallels histological progression in breast carcinogenesis
por: Cummings, M C, et al.
Publicado: (2000)

Recurrent Chromosomal Copy Number Alterations in Sporadic Chordomas
por: Le, Long Phi, et al.
Publicado: (2011)

Functional Copy-Number Alterations in Cancer
por: Taylor, Barry S., et al.
Publicado: (2008)

Detection of cell‐free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients
por: Mouliere, Florent, et al.
Publicado: (2018)

Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients
por: Wallander, Karin, et al.
Publicado: (2021)

Longitudinal Copy-Number Alteration Analysis in Plasma Cell-Free DNA of Neuroendocrine Neoplasms is a Novel Specific Biomarker for Diagnosis, Prognosis, and Follow-up
por: Boons, Gitta, et al.
Publicado: (2022)

Copy number variations and their effect on the plasma proteome
por: Schmitz, Daniel, et al.
Publicado: (2023)

Urinary Exosomal and cell-free DNA Detects Somatic Mutation and Copy Number Alteration in Urothelial Carcinoma of Bladder
por: Lee, Dong Hyeon, et al.
Publicado: (2018)

Copy Number Alterations and Methylation in Ewing's Sarcoma
por: Jahromi, Mona S., et al.
Publicado: (2011)

Coping with cancer genes altered by copy number
por: Wolf, Natalie K., et al.
Publicado: (2015)

Signatures of copy number alterations in human cancer
por: Steele, Christopher D., et al.
Publicado: (2022)

Gamma Knife Radiosurgery does not alter the copy number aberration profile in sporadic vestibular schwannoma
por: Håvik, Aril Løge, et al.
Publicado: (2020)

Copy number variations alter methylation and parallel IGF2 overexpression in adrenal tumors
por: Nielsen, Helene Myrtue, et al.
Publicado: (2015)

Increased copy number of the target gene squalene monooxygenase as the main resistance mechanism to terbinafine in Leishmania infantum()
por: Potvin, Jade-Éva, et al.
Publicado: (2023)

Individual and combined effects of DNA methylation and copy number alterations on miRNA expression in breast tumors
por: Aure, Miriam Ragle, et al.
Publicado: (2013)

A systematic comparison of copy number alterations in four types of female cancer
por: Kaveh, Fatemeh, et al.
Publicado: (2016)

Mitochondrial DNA Copy Number Is Associated With Treatment Response and Cognitive Function in Euthymic Bipolar Patients Receiving Valproate
por: Chang, Cheng-Chen, et al.
Publicado: (2022)

Copy number alterations in urothelial carcinomas: their clinicopathological significance and correlation with DNA methylation alterations
por: Nishiyama, Naotaka, et al.
Publicado: (2011)

Cannot write session to /tmp/vufind_sessions/sess_luslga5tg9mrujo87qo7p8o61p