Cargando…

Non-invasive prenatal diagnosis of thalassemia through multiplex PCR, target capture and next-generation sequencing

Prenatal clinical detection of thalassemia involves gap-PCR and reverse dot blot (RDB) analysis of fetal DNA acquired through invasive methods. The present study aimed to develop a non-invasive prenatal diagnostic method for thalassemia based on next-generation sequencing (NGS). A total of eight fam...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yang, Xu, Ye, Yanchou, Fan, Dongmei, Lin, Sheng, Li, Ming, Hou, Hongying, Zhang, Jun, Yang, Xuexi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2020
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7339645/ https://www.ncbi.nlm.nih.gov/pubmed/32627040 http://dx.doi.org/10.3892/mmr.2020.11234

Ejemplares similares

Multiplex PCR and Next Generation Sequencing for the Non-Invasive Detection of Bladder Cancer
por: Ward, Douglas G., et al.
Publicado: (2016)

Droplet-based digital PCR for non-invasive prenatal genetic diagnosis of α and β-thalassemia
por: Sawakwongpra, Kritchakorn, et al.
Publicado: (2021)

Dissecting Genomic Aberrations in Myeloproliferative Neoplasms by Multiplex-PCR and Next Generation Sequencing
por: Kirschner, Martin M. J., et al.
Publicado: (2015)

Evaluation of Ion Torrent next-generation sequencing for thalassemia diagnosis
por: Chen, Peisong, et al.
Publicado: (2020)

Next-Generation Sequencing (NGS) and Third-Generation Sequencing (TGS) for the Diagnosis of Thalassemia
por: Hassan, Syahzuwan, et al.
Publicado: (2023)

Prenatal Diagnosis of β-Thalassemias and Hemoglobinopathies.
por: Rosatelli, Maria Cristina, et al.
Publicado: (2009)

Non Invasive Prenatal Diagnosis of Aneuploidy: Next Generation Sequencing or Fetal DNA Enrichment?
por: Webb, A, et al.
Publicado: (2012)

Phylogenetic Properties of 50 Nuclear Loci in Medicago (Leguminosae) Generated Using Multiplexed Sequence Capture and Next-Generation Sequencing
por: de Sousa, Filipe, et al.
Publicado: (2014)

Multiplex PCR-based next generation sequencing as a novel, targeted and accurate molecular approach for periprosthetic joint infection diagnosis
por: Huang, Changyu, et al.
Publicado: (2023)

Multiplex PCR−Based Next-Generation Sequencing and Global Diversity of Seoul Virus in Humans and Rats
por: Kim, Won-Keun, et al.
Publicado: (2018)

Next-generation molecular diagnostics: Leveraging digital technologies to enhance multiplexing in real-time PCR
por: Kreitmann, Louis, et al.
Publicado: (2023)

Next Generation Sequencing Based Multiplex Long-Range PCR for Routine Genotyping of Autoinflammatory Disorders
por: Guzel, Ferhat, et al.
Publicado: (2021)

Invasive molecular prenatal diagnosis of alpha and beta thalassemia among Hakka pregnant women
por: Wu, Heming, et al.
Publicado: (2018)

Applications of next generation sequencing in the screening and diagnosis of thalassemia: A mini-review
por: Suhaimi, Syahirah Amnani, et al.
Publicado: (2022)

Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene
por: Tian, Yongan, et al.
Publicado: (2021)

Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation
por: Emms, Alexandra, et al.
Publicado: (2022)

Novel One-Step Multiplex PCR-Based Method for HLA Typing and Preimplantational Genetic Diagnosis of β-Thalassemia
por: Fernández, Raquel M., et al.
Publicado: (2013)

Correction: Phylogenetic Properties of 50 Nuclear Loci in Medicago (Leguminosae) Generated Using Multiplexed Sequence Capture and Next-Generation Sequencing
Publicado: (2015)

Anchored Multiplex PCR Custom Melanoma Next Generation Sequencing Panel for Analysis of Circulating Tumor DNA
por: Diefenbach, Russell J., et al.
Publicado: (2022)

Next generation multiplexing for digital PCR using a novel melt-based hairpin probe design
por: Edwards, Rebecca L., et al.
Publicado: (2023)

Multiplexed DNA Sequence Capture of Mitochondrial Genomes Using PCR Products
por: Maricic, Tomislav, et al.
Publicado: (2010)

Role of Fetal Blood Sampling in the Prenatal Diagnosis of Thalassemia
por: Xie, Xing-Mei, et al.
Publicado: (2023)

Next-generation sequencing analysis of the molecular spectrum of thalassemia in Southern Jiangxi, China
por: Yang, Tong, et al.
Publicado: (2023)

Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion
por: Jomoui, Wittaya, et al.
Publicado: (2023)

Diagnosis for choroideremia in a large Chinese pedigree by next-generation sequencing (NGS) and non-invasive prenatal testing (NIPT)
por: Zhu, Li, et al.
Publicado: (2017)

Genotyping and Molecular Diagnosis of Hepatitis A Virus in Human Clinical Samples Using Multiplex PCR-Based Next-Generation Sequencing
por: Lee, Geum-Young, et al.
Publicado: (2022)

A novel method for the multiplexed target enrichment of MinION next generation sequencing libraries using PCR-generated baits
por: Karamitros, Timokratis, et al.
Publicado: (2015)

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants
por: Jiang, Fan, et al.
Publicado: (2023)

Comprehensive Analysis of Disease-Related Genes in Chronic Lymphocytic Leukemia by Multiplex PCR-Based Next Generation Sequencing
por: Vollbrecht, Claudia, et al.
Publicado: (2015)

Phylogeographic analysis of hemorrhagic fever with renal syndrome patients using multiplex PCR-based next generation sequencing
por: Kim, Won-Keun, et al.
Publicado: (2016)

Confirming Multiplex RT-qPCR Use in COVID-19 with Next-Generation Sequencing: Strategies for Epidemiological Advantage
por: Carpenter, Rob E., et al.
Publicado: (2022)

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)

Hypermethylation of IGSF4 gene for noninvasive prenatal diagnosis of thalassemia
por: Gao, Tian, et al.
Publicado: (2012)

In response to “Role of Fetal Blood Sampling in the Prenatal Diagnosis of Thalassemia”
por: Dündar Yenilmez, Ebru
Publicado: (2023)

Molecular Diagnosis of Putative Stargardt Disease by Capture Next Generation Sequencing
por: Zhang, Xiao, et al.
Publicado: (2014)

Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis
por: Almes, Marion, et al.
Publicado: (2022)

Next‐generation sequencing improves molecular epidemiological characterization of thalassemia in Chenzhou Region, P.R. China
por: Zhang, Haoqing, et al.
Publicado: (2019)

Non-invasive prenatal testing for fetal Ss, Kidd, and CTL2 blood group prediction by multiplex digital droplet PCR
por: Wang, Yufeng, et al.
Publicado: (2023)

Utility of Select Gene Mutation Detection in Tumors by the Idylla Rapid Multiplex PCR Platform in Comparison to Next-Generation Sequencing
por: Nkosi, Dingani, et al.
Publicado: (2022)

Non-Invasive Prenatal Diagnosis of Lethal Skeletal Dysplasia by Targeted Capture Sequencing of Maternal Plasma
por: Dan, Shan, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_fpjtsd2jsr4eip2an56rmto55l