Cargando…

Simple Detection of Large InDeLS by DHPLC: The ACE Gene as a Model

Insertion-deletion polymorphism (InDeL) is the second most frequent type of genetic variation in the human genome. For the detection of large InDeLs, researchers usually resort to either PCR gel analysis or RFLP, but these are time consuming and dependent on human interpretation. Therefore, a more e...

Descripción completa

Detalles Bibliográficos
Autores principales:	Koyama, Renata Guedes, Castro, Rosa M. R. P. S., De Mello, Marco Túlio, Tufik, Sergio, Pedrazzoli, Mario
Formato:	Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2008
Materias:	Methodology Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2358980/ https://www.ncbi.nlm.nih.gov/pubmed/18475319 http://dx.doi.org/10.1155/2008/562183

Ejemplares similares

DHPLC technology for high-throughput detection of mutations in a durum wheat TILLING population
por: Colasuonno, Pasqualina, et al.
Publicado: (2016)

IndelsRNAmute: predicting deleterious multiple point substitutions and indels mutations
por: Churkin, Alexander, et al.
Publicado: (2022)

Progressive multiple sequence alignment with indel evolution
por: Maiolo, Massimo, et al.
Publicado: (2018)

Minimum InDel pattern analysis of the Zika virus
por: Lee, Hyeji, et al.
Publicado: (2018)

Detection of mutations in the dystrophin gene via automated DHPLC screening and direct sequencing
por: Bennett, Richard R, et al.
Publicado: (2001)

Calling large indels in 1047 Arabidopsis with IndelEnsembler
por: Liu, Dong-Xu, et al.
Publicado: (2021)

Incorporating indel information into phylogeny estimation for rapidly emerging pathogens
por: Redelings, Benjamin D, et al.
Publicado: (2007)

Identification of genomic indels and structural variations using split reads
por: Zhang, Zhengdong D, et al.
Publicado: (2011)

GapCoder automates the use of indel characters in phylogenetic analysis
por: Young, Nelson D, et al.
Publicado: (2003)

Accurate indel prediction using paired-end short reads
por: Grimm, Dominik, et al.
Publicado: (2013)

UDiTaS™, a genome editing detection method for indels and genome rearrangements
por: Giannoukos, Georgia, et al.
Publicado: (2018)

Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays
por: Bischoff, Steve R, et al.
Publicado: (2008)

Mutation detection in familial and sporadic breast cancers by denaturing high-performance liquid chromatography (DHPLC)
por: Betz, B, et al.
Publicado: (2001)

Efficient IDUA Gene Mutation Detection with Combined Use of dHPLC and Dried Blood Samples
por: Ribeiro, Diogo, et al.
Publicado: (2013)

InDel marker detection by integration of multiple softwares using machine learning techniques
por: Yang, Jianqiu, et al.
Publicado: (2016)

Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy
por: D'Apice, Maria Rosaria, et al.
Publicado: (2004)

Lack of Association Between ACE Indel Polymorphism and Cardiorespiratory Fitness in Physically Active and Sedentary Young Women
por: Verlengia, Rozangela, et al.
Publicado: (2014)

Vindel: a simple pipeline for checking indel redundancy
por: Li, Zhiyi, et al.
Publicado: (2014)

DHPLC Screening of ATM Gene in Italian Patients Affected by Ataxia-Telangiectasia: Fourteen Novel ATM Mutations
por: Magliozzi, Monia, et al.
Publicado: (2006)

DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis
por: Dastsooz, Hassan, et al.
Publicado: (2013)

LS-NMF: A modified non-negative matrix factorization algorithm utilizing uncertainty estimates
por: Wang, Guoli, et al.
Publicado: (2006)

Evaluation and optimisation of indel detection workflows for ion torrent sequencing of the BRCA1 and BRCA2 genes
por: Yeo, Zhen Xuan, et al.
Publicado: (2014)

Classification based on extensions of LS-PLS using logistic regression: application to clinical and multiple genomic data
por: Bazzoli, Caroline, et al.
Publicado: (2018)

Discovery and application of insertion-deletion (INDEL) polymorphisms for QTL mapping of early life-history traits in Atlantic salmon
por: Vasemägi, Anti, et al.
Publicado: (2010)

A single blastocyst assay optimized for detecting CRISPR/Cas9 system-induced indel mutations in mice
por: Sakurai, Takayuki, et al.
Publicado: (2014)

A simplified method for identifying early CRISPR-induced indels in zebrafish embryos using High Resolution Melting analysis
por: Samarut, Éric, et al.
Publicado: (2016)

Mapping the Expert Mind: Integration Method for Revising the ACES Medical Simulation Curriculum
por: Cardinal, Pierre, et al.
Publicado: (2020)

MCALIGN2: Faster, accurate global pairwise alignment of non-coding DNA sequences based on explicit models of indel evolution
por: Wang, Jun, et al.
Publicado: (2006)

Efficient recovery of proteins from multiple source samples after trizol((®)) or trizol((®))LS RNA extraction and long-term storage
por: Simões, André ES, et al.
Publicado: (2013)

Indel Reliability in Indel-Based Phylogenetic Inference
por: Ashkenazy, Haim, et al.
Publicado: (2014)

Detection of candidate gene LsACOS5 and development of InDel marker for male sterility by ddRAD-seq and resequencing analysis in lettuce
por: Seki, Kousuke
Publicado: (2022)

Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation
por: Mutai, Hideki, et al.
Publicado: (2011)

THE LS-ANTIGEN OF VACCINIA : IV. CHEMICAL ANALYSIS OF LS AND THE EFFECT OF CHYMOTRYPSIN ON LS
por: Smadel, Joseph E., et al.
Publicado: (1943)

Health Information Technologies—Academic and Commercial Evaluation (HIT-ACE) methodology: description and application to clinical feedback systems
por: Lyon, Aaron R., et al.
Publicado: (2016)

UPS-indel: a Universal Positioning System for Indels
por: Hasan, Mohammad Shabbir, et al.
Publicado: (2017)

Rapid and Accurate Approach for Screening of Microsatellite Unstable Tumours Using Quasimonomorphic Mononucleotide Repeats and Denaturating High Performance Liquid Chromatography (DHPLC)
por: Berginc, Gašper, et al.
Publicado: (2009)

Erratum to “Screening for polymorphisms in the AANAT gene and their association with extreme diurnal preference” [Sleep Sci. 6 (4) (2013) 141–145
por: Koike, Bruna Del Vechio, et al.
Publicado: (2014)

Sleep disorder or simple sleep ontogeny? Tendency for morningness is associated with worse sleep quality in the elderly
por: Barbosa, A.A., et al.
Publicado: (2016)

Simple steps to develop trial follow-up procedures
por: McCarthy, Ona, et al.
Publicado: (2016)

Atraumatic Flexor tendon retrieval- a simple method
por: Ozturk, Muhammed Besir, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_51rh7i4drti9fiteo83sgsa7o9