Cargando…

Comparative Studies of Copy Number Variation Detection Methods for Next-Generation Sequencing Technologies

Copy number variation (CNV) has played an important role in studies of susceptibility or resistance to complex diseases. Traditional methods such as fluorescence in situ hybridization (FISH) and array comparative genomic hybridization (aCGH) suffer from low resolution of genomic regions. Following t...

Descripción completa

Detalles Bibliográficos
Autores principales:	Duan, Junbo, Zhang, Ji-Gang, Deng, Hong-Wen, Wang, Yu-Ping
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3604020/ https://www.ncbi.nlm.nih.gov/pubmed/23527109 http://dx.doi.org/10.1371/journal.pone.0059128

Ejemplares similares

CNV-TV: A robust method to discover copy number variation from short sequencing reads
por: Duan, Junbo, et al.
Publicado: (2013)

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

Comparative study of whole exome sequencing-based copy number variation detection tools
por: Zhao, Lanling, 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)

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

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

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)

Evaluation of Next Generation Sequencing for Detecting HER2 Copy Number in Breast and Gastric Cancers
por: Niu, Dongfeng, et al.
Publicado: (2020)

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

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)

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)

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)

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

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

Detection of Single-Nucleotide and Copy Number Defects Underlying Hyperphenylalaninemia by Next-Generation Sequencing
por: Tendi, Elisabetta Anna, et al.
Publicado: (2023)

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)

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

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)

RKDOSCNV: A Local Kernel Density-Based Approach to the Detection of Copy Number Variations by Using Next-Generation Sequencing Data
por: Liu, Guojun, et al.
Publicado: (2020)

Evaluation of copy number variant detection from panel‐based next‐generation sequencing data
por: Yao, Ruen, et al.
Publicado: (2018)

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)

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

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

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)

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)

Cannot write session to /tmp/vufind_sessions/sess_vn763niek4jkib5ja5pkievmbt