Cargando…

Next generation sequencing identifies recurrent copy number variations in invasive breast carcinomas from Ghana

African and African American (AA) women have a higher incidence of triple negative breast cancers (TNBC) with high histological grade and aggressive clinical behavior, but the reasons are not fully understood. We recently found that the oncogenic protein EZH2 is overexpressed in Ghanaian breast canc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Anwar, Talha, Rufail, Miguel L., Djomehri, Sabra, Gonzalez, Maria E., Lorena Lazo, De La Vega, Tomlins, Scott A., Newman, Lisa A., Kleer, Celina G.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390688/ https://www.ncbi.nlm.nih.gov/pubmed/32152520 http://dx.doi.org/10.1038/s41379-020-0515-2

Ejemplares similares

Copy number variation detection using next generation sequencing read counts
por: Wang, Heng, et al.
Publicado: (2014)

Comparative Studies of Copy Number Variation Detection Methods for Next-Generation Sequencing Technologies
por: Duan, Junbo, et al.
Publicado: (2013)

Human Y chromosome copy number variation in the next generation sequencing era and beyond
por: Massaia, Andrea, et al.
Publicado: (2017)

Estimates of penetrance for recurrent pathogenic copy-number variations
por: Rosenfeld, Jill A., et al.
Publicado: (2013)

Deleted copy number variation of Hanwoo and Holstein using next generation sequencing at the population level
por: Shin, Dong-Hyun, et al.
Publicado: (2014)

Global copy number analyses by next generation sequencing provide insight into pig genome variation
por: Jiang, Jicai, et al.
Publicado: (2014)

Use of next-generation sequencing to detect LDLR gene copy number variation in familial hypercholesterolemia
por: Iacocca, Michael A., et al.
Publicado: (2017)

Identification of copy number variation in French dairy and beef breeds using next-generation sequencing
por: Letaief, Rabia, et al.
Publicado: (2017)

A Deep Learning Approach for Detecting Copy Number Variation in Next-Generation Sequencing Data
por: Hill, Tom, et al.
Publicado: (2019)

Detecting copy number variation in next generation sequencing data from diagnostic gene panels
por: Singh, Ashish Kumar, et al.
Publicado: (2021)

Genome-wide patterns of copy number variation in the diversified chicken genomes using next-generation sequencing
por: Yi, Guoqiang, et al.
Publicado: (2014)

Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing
por: Wang, Jing, et al.
Publicado: (2018)

MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data
por: Zhao, Haiyong, et al.
Publicado: (2020)

Chromosomal copy number variations in products of conception from spontaneous abortion by next-generation sequencing technology
por: Dai, Rulin, et al.
Publicado: (2019)

A Cluster-Based Approach for the Discovery of Copy Number Variations From Next-Generation Sequencing Data
por: Liu, Guojun, et al.
Publicado: (2021)

Copy number variation characterization and possible candidate genes in miscarriage and stillbirth by next‐generation sequencing analysis
por: Zhang, Xia, et al.
Publicado: (2021)

CNV-PCC: An efficient method for detecting copy number variations from next-generation sequencing data
por: Zhang, Tong, et al.
Publicado: (2022)

Detection of copy number variations based on a local distance using next-generation sequencing data
por: Liu, Guojun, et al.
Publicado: (2023)

Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder
por: Rucker, James J.H., et al.
Publicado: (2016)

Recurrent copy number variations in the human fungal pathogen Candida parapsilosis
por: Selmecki, Anna
Publicado: (2023)

Copy number variations and cancer
por: Shlien, Adam, et al.
Publicado: (2009)

Copy number variations and stroke
por: Colaianni, Valeria, et al.
Publicado: (2016)

Copy Number Variations and Schizophrenia
por: Szecówka, Kamila, et al.
Publicado: (2022)

Copy Number Variation and Osteoporosis
por: Lovšin, Nika
Publicado: (2023)

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives
por: Zhao, Min, et al.
Publicado: (2013)

Computational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challenges
por: Liu, Biao, et al.
Publicado: (2013)

Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome
por: Morita, Kei-ichi, et al.
Publicado: (2015)

Non-invasive Analysis of Genomic Copy Number Variation in Patients with Hepatocellular Carcinoma by Next Generation DNA Sequencing
por: Xu, Hongtao, et al.
Publicado: (2015)

Chromosomal copy number variation analysis by next generation sequencing confirms ploidy stability in Trypanosoma brucei subspecies
por: Almeida, Laila Viana, et al.
Publicado: (2018)

SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data
por: Chen, Yong, et al.
Publicado: (2017)

A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples
por: Zhou, Xiya, et al.
Publicado: (2021)

HBOS-CNV: A New Approach to Detect Copy Number Variations From Next-Generation Sequencing Data
por: Guo, Yang, et al.
Publicado: (2021)

A Density Peak-Based Method to Detect Copy Number Variations From Next-Generation Sequencing Data
por: Xie, Kun, et al.
Publicado: (2021)

A shortest path-based approach for copy number variation detection from next-generation sequencing data
por: Liu, Guojun, et al.
Publicado: (2023)

Allele-specific copy number profiling by next-generation DNA sequencing
por: Chen, Hao, et al.
Publicado: (2015)

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

Interactive analysis of large cancer copy number studies with Copy Number Explorer
por: Newman, Scott
Publicado: (2015)

Analysis of copy number variations and possible candidate genes in spontaneous abortion by copy number variation sequencing
por: Bai, Wei, et al.
Publicado: (2023)

Genome Wide Association Analysis of Copy Number Variation in Recurrent Depressive Disorder
por: Rucker, James J.H., et al.
Publicado: (2011)

Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses
por: Sheng, Yan-Ran, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_0tnn3uvret6aigpt6ea8k9ukbj