Cargando…

Non-invasive Analysis of Genomic Copy Number Variation in Patients with Hepatocellular Carcinoma by Next Generation DNA Sequencing

To explore new molecular diagnosis approaches for early detection and differential diagnosis of hepatocellular carcinoma (HCC), we analyzed genomic copy number variations (CNV) using plasma cell-free DNA from patients with HCC by next generation DNA sequencing. Plasma samples from 31 patients with H...

Descripción completa

Detalles Bibliográficos
Autores principales:	Xu, Hongtao, Zhu, Xia, Xu, Zulong, Hu, Yue, Bo, Shiping, Xing, Tongjing, Zhu, Kuichun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Ivyspring International Publisher 2015
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4317760/ https://www.ncbi.nlm.nih.gov/pubmed/25663942 http://dx.doi.org/10.7150/jca.10747

Ejemplares similares

Next generation sequencing identifies recurrent copy number variations in invasive breast carcinomas from Ghana
por: Anwar, Talha, et al.
Publicado: (2020)

Copy number variation detection using next generation sequencing read counts
por: Wang, Heng, 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)

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

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

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)

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)

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)

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

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)

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)

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

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)

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

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)

Copy number variation in the bovine genome
por: Fadista, João, et al.
Publicado: (2010)

Genome-wide copy number variations in Oryza sativa L.
por: Yu, Ping, et al.
Publicado: (2013)

Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing
por: Alkan, Can, et al.
Publicado: (2009)

Chromosomal Instability Estimation Based on Next Generation Sequencing and Single Cell Genome Wide Copy Number Variation Analysis
por: Greene, Stephanie B., et al.
Publicado: (2016)

Novel copy number variation of POMGNT1 associated with muscle-eye-brain disease detected by next-generation sequencing
por: Fu, Xiaona, et al.
Publicado: (2017)

CNspector: a web-based tool for visualisation and clinical diagnosis of copy number variation from next generation sequencing
por: Markham, John F., et al.
Publicado: (2019)

Improving high-resolution copy number variation analysis from next generation sequencing using unique molecular identifiers
por: Viailly, Pierre-Julien, et al.
Publicado: (2021)

Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation Sequencing
por: Fan, Lei, et al.
Publicado: (2020)

Heteroplasmy and Copy Number Variations of Mitochondria in 88 Hepatocellular Carcinoma Individuals
por: Li, Weiyang, et al.
Publicado: (2017)

Copy number variations of MMP-9 are prognostic biomarkers for hepatocellular carcinoma
por: Yu, Xi, et al.
Publicado: (2020)

Role of chromosome 1q copy number variation in hepatocellular carcinoma
por: Jacobs, Nathan R, et al.
Publicado: (2021)

Copy number variations (CNVs) and karyotyping analysis in males with azoospermia and oligospermia
por: Xin, Xing, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_c4kk8c2odfkd0ae86p5jld4hhh