Cargando…

Detection of copy number variations based on a local distance using next-generation sequencing data

As one of the main types of structural variation in the human genome, copy number variation (CNV) plays an important role in the occurrence and development of human cancers. Next-generation sequencing (NGS) technology can provide base-level resolution, which provides favorable conditions for the acc...

Descripción completa

Detalles Bibliográficos
Autores principales:	Liu, Guojun, Yang, Hongzhi, He, Zongzhen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2023
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10556732/ https://www.ncbi.nlm.nih.gov/pubmed/37811148 http://dx.doi.org/10.3389/fgene.2023.1147761

Ejemplares similares

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

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)

MFCNV: A New Method to Detect Copy Number Variations From Next-Generation Sequencing Data
por: Zhao, Haiyong, 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)

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)

CNV-MEANN: A Neural Network and Mind Evolutionary Algorithm-Based Detection of Copy Number Variations From Next-Generation Sequencing Data
por: Huang, Tihao, et al.
Publicado: (2021)

A Pipeline for Reconstructing Somatic Copy Number Alternation’s Subclonal Population-Based Next-Generation Sequencing Data
por: Chu, Yanshuo, et al.
Publicado: (2020)

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

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)

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

Next Generation Sequencing Identify Rare Copy Number Variants in Non-syndromic Patent Ductus Arteriosus
por: Chen, Bo, et al.
Publicado: (2020)

Inferring Variation in Copy Number Using High Throughput Sequencing Data in R
por: Knaus, Brian J., et al.
Publicado: (2018)

Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family Trios
por: Liu, Yichuan, et al.
Publicado: (2019)

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

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

Clinical massively parallel next-generation sequencing analysis of 409 cancer-related genes for mutations and copy number variations in solid tumours
por: Singh, R R, et al.
Publicado: (2014)

A Survey of Copy Number Variation in the Porcine Genome Detected From Whole-Genome Sequence
por: Keel, Brittney N., et al.
Publicado: (2019)

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

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

Detection of Copy Number Alterations Using Single Cell Sequencing
por: Knouse, Kristin A., et al.
Publicado: (2017)

Copy Number Variation Analysis of Euploid Pregnancy Loss
por: Gu, Chongjuan, et al.
Publicado: (2022)

Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach
por: Bhai, Pratibha, et al.
Publicado: (2021)

Editorial: Copy Number Variation in Rare Disorders
por: Komlósi, Katalin, et al.
Publicado: (2022)

A novel scatterplot-based method to detect copy number variation (CNV)
por: Qiao, Jia-Lu, et al.
Publicado: (2023)

Comprehensive Analysis of Copy Number Variations in Kidney Cancer by Single-Cell Exome Sequencing
por: Zhou, Wenyang, et al.
Publicado: (2020)

Application of Copy Number Variation Detection to Fetal Diagnosis of Echogenic Intracardiac Focus During Pregnancy
por: Song, Yaxian, et al.
Publicado: (2021)

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

Detection of Pathogenic Microbe Composition Using Next-Generation Sequencing Data
por: Zhao, Haiyong, et al.
Publicado: (2020)

Copy Number Variation Identification on 3,800 Alzheimer’s Disease Whole Genome Sequencing Data from the Alzheimer’s Disease Sequencing Project
por: Lee, Wan-Ping, et al.
Publicado: (2021)

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

Germline Copy Number Variation and Ovarian Cancer Survival
por: Fridley, Brooke L., et al.
Publicado: (2012)

Comprehensive Evaluation of Non-invasive Prenatal Screening to Detect Fetal Copy Number Variations
por: Wang, Jing, et al.
Publicado: (2021)

Genome-Wide Detection of Copy Number Variations and Their Association With Distinct Phenotypes in the World’s Sheep
por: Salehian-Dehkordi, Hosein, et al.
Publicado: (2021)

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)

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

Copy Number Variation Mapping and Genomic Variation of Autochthonous and Commercial Turkey Populations
por: Strillacci, Maria G., et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_s1okpc3sq5r98asp2chh5ida51