Cargando…

Corrigendum: Sequence and Structure Characteristics of 22 Deletion Breakpoints in Intron 44 of the DMD Gene Based on Long-Read Sequencing

Detalles Bibliográficos
Autores principales:	Geng, Chang, Tong, Yuanren, Zhang, Siwen, Ling, Chao, Wu, Xin, Wang, Depeng, Dai, Yi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2021
Materias:	Genetics
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8241914/ https://www.ncbi.nlm.nih.gov/pubmed/34220967 http://dx.doi.org/10.3389/fgene.2021.706540

Ejemplares similares

Sequence and Structure Characteristics of 22 Deletion Breakpoints in Intron 44 of the DMD Gene Based on Long-Read Sequencing
por: Geng, Chang, et al.
Publicado: (2021)

Location of Balanced Chromosome-Translocation Breakpoints by Long-Read Sequencing on the Oxford Nanopore Platform
por: Hu, Liang, et al.
Publicado: (2020)

Breakpoint junction features of seven DMD deletion mutations
por: Keegan, Niall P., et al.
Publicado: (2019)

Long-Read Sequencing Revealed Extragenic and Intragenic Duplications of Exons 56–61 in DMD in an Asymptomatic Male and a DMD Patient
por: Bai, Ying, et al.
Publicado: (2022)

Detection of pericentric inversion with breakpoint in DMD by whole genome sequencing
por: Zaum, Ann‐Kathrin, et al.
Publicado: (2022)

Novel Intronic Mutations Introduce Pseudoexons in DMD That Cause Muscular Dystrophy in Patients
por: Lu, Xinguo, et al.
Publicado: (2021)

High-resolution mapping of reciprocal translocation breakpoints using long-read sequencing
por: Chow, Judy F.C., et al.
Publicado: (2019)

Case report: a novel deep intronic splice-altering variant in DMD as a cause of Becker muscular dystrophy
por: Berntsson, Shala Ghaderi, et al.
Publicado: (2023)

Corrigendum: Evaluation of CircRNA sequence assembly methods using long reads
por: Zhang, Jingjing, et al.
Publicado: (2023)

Fast detection of deletion breakpoints using quantitative PCR
por: Abildinova, Gulshara, et al.
Publicado: (2016)

Nanopore long-read next-generation sequencing for detection of mitochondrial DNA large-scale deletions
por: Frascarelli, Chiara, et al.
Publicado: (2023)

Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis
por: Pei, Zhenle, et al.
Publicado: (2022)

SRBreak: A Read-Depth and Split-Read Framework to Identify Breakpoints of Different Events Inside Simple Copy-Number Variable Regions
por: Nguyen, Hoang T., et al.
Publicado: (2016)

Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
por: Sadikovic, Bekim, et al.
Publicado: (2010)

Novel Partial Exon 51 Deletion in the Duchenne Muscular Dystrophy Gene Identified via Whole Exome Sequencing and Long-Read Whole-Genome Sequencing
por: Li, Qianqian, et al.
Publicado: (2021)

MATCHCLIP: locate precise breakpoints for copy number variation using CIGAR string by matching soft clipped reads
por: Wu, Yinghua, et al.
Publicado: (2013)

Frequency of Intron 22 Inversion in Severe Hemophilia A Patients
por: Ashfaq, Javeria, et al.
Publicado: (2022)

Profiling the Genome-Wide Landscape of Short Tandem Repeats by Long-Read Sequencing
por: Liu, Zhenhua, et al.
Publicado: (2022)

Linked-Read Whole Genome Sequencing Solves a Double DMD Gene Rearrangement
por: Onore, Maria Elena, et al.
Publicado: (2021)

Association of G-quadruplex forming sequences with human mtDNA deletion breakpoints
por: Dong, Dawei W, et al.
Publicado: (2014)

Correction: Sequence Homology at the Breakpoint and Clinical Phenotype of Mitochondrial DNA Deletion Syndromes
por: Sadikovic, Bekim, et al.
Publicado: (2017)

Target-capture full-length double-stranded cDNA long-read sequencing through Nanopore revealed novel intron retention in patient with tuberous sclerosis complex
por: Ura, Hiroki, et al.
Publicado: (2023)

Long-Read Sequencing Emerging in Medical Genetics
por: Mantere, Tuomo, et al.
Publicado: (2019)

Deciphering the exact breakpoints of structural variations using long sequencing reads with DeBreak
por: Chen, Yu, et al.
Publicado: (2023)

Identification of a Novel Deep Intronic Variant by Whole Genome Sequencing Combined With RNA Sequencing in a Chinese Patient With Menkes Disease
por: Zhi, Xiufang, et al.
Publicado: (2022)

Genotypes and Phenotypes of DMD Small Mutations in Chinese Patients With Dystrophinopathies
por: Wang, Liang, et al.
Publicado: (2019)

An intronic polymorphic deletion in the PTEN gene: implications for molecular diagnostic testing
por: Sandell, S, et al.
Publicado: (2013)

Long-Read Sequencing Revealed an Extensive Transcript Complexity in Herpesviruses
por: Tombácz, Dóra, et al.
Publicado: (2018)

Editorial: Long-read sequencing—Pitfalls, benefits and success stories
por: Wohlers, Inken, et al.
Publicado: (2023)

Translocation and deletion breakpoints in cancer genomes are associated with potential non-B DNA-forming sequences
por: Bacolla, Albino, et al.
Publicado: (2016)

Case report: Long-read sequencing identified a novel 14.9-kb deletion of the α-globin gene locus in a family with α-thalassemia in China
por: Yuan, Yan, et al.
Publicado: (2023)

DINTD: Detection and Inference of Tandem Duplications From Short Sequencing Reads
por: Dong, Jinxin, et al.
Publicado: (2020)

Whole Genome Assembly of Human Papillomavirus by Nanopore Long-Read Sequencing
por: Yang, Shuaibing, et al.
Publicado: (2022)

Evaluation of CircRNA Sequence Assembly Methods Using Long Reads
por: Zhang, Jingjing, et al.
Publicado: (2022)

LCAT: an isoform-sensitive error correction for transcriptome sequencing long reads
por: Zhu, Wufei, et al.
Publicado: (2023)

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome
por: Du, Qiumei, et al.
Publicado: (2020)

Sequence Read Depth Analysis of a Monophyletic Cluster of Y Chromosomes Characterized by Structural Rearrangements in the AZFc Region Resulting in DYS448 Deletion and DYF387S1 Duplication
por: Ravasini, Francesco, et al.
Publicado: (2021)

The Function of Introns
por: Chorev, Michal, et al.
Publicado: (2012)

Co-barcoded sequence reads from long DNA fragments: a cost-effective solution for “perfect genome” sequencing
por: Peters, Brock A., et al.
Publicado: (2015)

Phenotype Driven Analysis of Whole Genome Sequencing Identifies Deep Intronic Variants that Cause Retinal Dystrophies by Aberrant Exonization
por: Di Scipio, Matteo, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_gqp4ms5hk2438t57kv53each42