Cargando…

Correction: Clonality analysis of pulmonary tumors by genome-wide copy number profiling

Detalles Bibliográficos
Autores principales:	Vincenten, Julien P. L., van Essen, Hendrik F., Lissenberg-Witte, Birgit I., Bulkmans, Nicole W. J., Krijgsman, Oscar, Sie, Daoud, Eijk, Paul P., Smit, Egbert F., Ylstra, Bauke, Thunnissen, Erik
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2019
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6863545/ https://www.ncbi.nlm.nih.gov/pubmed/31743370 http://dx.doi.org/10.1371/journal.pone.0225733

Ejemplares similares

Clonality analysis of pulmonary tumors by genome-wide copy number profiling
por: Vincenten, Julien P. L., et al.
Publicado: (2019)

FocalCall: An R Package for the Annotation of Focal Copy Number Aberrations
por: Krijgsman, Oscar, et al.
Publicado: (2014)

DNA copy number analysis of fresh and formalin-fixed specimens by shallow whole-genome sequencing with identification and exclusion of problematic regions in the genome assembly
por: Scheinin, Ilari, et al.
Publicado: (2014)

False positivity in break apart fluorescence in-situ hybridization due to polyploidy
por: van Gulik, Anna Lena, et al.
Publicado: (2023)

Focal Chromosomal Copy Number Aberrations Identify CMTM8 and GPR177 as New Candidate Driver Genes in Osteosarcoma
por: Both, Joeri, et al.
Publicado: (2014)

Chromosomal Copy Number Aberrations in Colorectal Metastases Resemble Their Primary Counterparts and Differences Are Typically Non-Recurrent
por: Mekenkamp, Leonie J. M., et al.
Publicado: (2014)

CopywriteR: DNA copy number detection from off-target sequence data
por: Kuilman, Thomas, et al.
Publicado: (2015)

Association of tumour and stroma PD-1, PD-L1, CD3, CD4 and CD8 expression with DCB and OS to nivolumab treatment in NSCLC patients pre-treated with chemotherapy
por: Niemeijer, Anna-Larissa Nadia, et al.
Publicado: (2020)

CGHpower: exploring sample size calculations for chromosomal copy number experiments
por: Scheinin, Ilari, et al.
Publicado: (2010)

Chromosomal copy number heterogeneity predicts survival rates across cancers
por: van Dijk, Erik, et al.
Publicado: (2021)

High number of chromosomal copy number aberrations inversely relates to t(11;19)(q21;p13) translocation status in mucoepidermoid carcinoma of the salivary glands
por: Matse, Johannes H., et al.
Publicado: (2017)

Reduced rate of copy number aberrations in mucinous colorectal carcinoma
por: Hugen, Niek, et al.
Publicado: (2015)

Copy-number signatures and mutational processes in ovarian carcinoma
por: Macintyre, Geoff, et al.
Publicado: (2018)

DNA copy number profiles of gastric cancer precursor lesions
por: Buffart, Tineke E, et al.
Publicado: (2007)

GeneBreak: detection of recurrent DNA copy number aberration-associated chromosomal breakpoints within genes
por: van den Broek, Evert, et al.
Publicado: (2017)

Clonal copy-number mosaicism in autoreactive T lymphocytes in diabetic NOD mice
por: Alriyami, Maha, et al.
Publicado: (2019)

Spatially resolved clonal copy number alterations in benign and malignant tissue
por: Erickson, Andrew, et al.
Publicado: (2022)

High resolution analysis of DNA copy-number aberrations of chromosomes 8, 13, and 20 in gastric cancers
por: Buffart, Tineke E., et al.
Publicado: (2009)

Breast tumor copy number aberration phenotypes and genomic instability
por: Fridlyand, Jane, et al.
Publicado: (2006)

Delineating copy number and clonal substructure in human tumors from single-cell transcriptomes
por: Gao, Ruli, et al.
Publicado: (2021)

Clonal evolution in UKE-1 cell line leading to an increase in JAK2 copy number
por: Buors, C, et al.
Publicado: (2012)

Punctuated Copy Number Evolution and Clonal Stasis in Triple-Negative Breast Cancer
por: Gao, Ruli, et al.
Publicado: (2016)

T-Cell Lymphoma Clonality by Copy Number Variation Analysis of T-Cell Receptor Genes
por: Oon, Ming Liang, et al.
Publicado: (2021)

The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research
por: Salgado, David, et al.
Publicado: (2020)

Tumor Atelectasis Gives Rise to a Solid Appearance in Pulmonary Adenocarcinomas on High-Resolution Computed Tomography
por: Ambrosi, Francesca, et al.
Publicado: (2020)

Clonal Patterns Between Pouch Neoplasia and Prior Colorectal Neoplasia in Inflammatory Bowel Disease Patients: An Exploratory Cohort Study
por: te Groen, Maarten, et al.
Publicado: (2023)

Genetically predicted telomere length is associated with clonal somatic copy number alterations in peripheral leukocytes
por: Brown, Derek W., et al.
Publicado: (2020)

Marie Curie – Genome Architecture in Relation to Disease
por: Ylstra, Bauke
Publicado: (2007)

Engineering large-scale chromosomal deletions by CRISPR-Cas9
por: Eleveld, Thomas F, et al.
Publicado: (2021)

TITAN: inference of copy number architectures in clonal cell populations from tumor whole-genome sequence data
por: Ha, Gavin, et al.
Publicado: (2014)

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain
por: Cai, Xuyu, et al.
Publicado: (2014)

FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing
por: Shen, Ronglai, et al.
Publicado: (2016)

Diagnosis of Fanconi Anemia: Mutation Analysis by Next-Generation Sequencing
por: Ameziane, Najim, et al.
Publicado: (2012)

DNA Copy Number Changes at 8q11–24 in Metastasized Colorectal Cancer
por: Buffart, T. E., et al.
Publicado: (2005)

Genomic profiling of stage II and III colon cancers reveals APC mutations to be associated with survival in stage III colon cancer patients
por: van den Broek, Evert, et al.
Publicado: (2016)

Reconstructing tumor clonal lineage trees incorporating single-nucleotide variants, copy number alterations and structural variations
por: Fu, Xuecong, et al.
Publicado: (2022)

A variational algorithm to detect the clonal copy number substructure of tumors from scRNA-seq data
por: De Falco, Antonio, et al.
Publicado: (2023)

Clonal somatic copy number altered driver events inform drug sensitivity in high-grade serous ovarian cancer
por: Martins, Filipe Correia, et al.
Publicado: (2022)

Somatic mutation in PIK3CA is a late event in cervical carcinogenesis
por: Verlaat, Wina, et al.
Publicado: (2015)

High Prevalence and Clinical Relevance of Genes Affected by Chromosomal Breaks in Colorectal Cancer
por: van den Broek, Evert, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_av0722tvh2g017s8it8dcbpi00