Cargando…

Cancer gene mutation discovery and detection using array-based resequencing

Detalles Bibliográficos
Autores principales:	Tengs, T, Lee, JC, Paez, JG, Zhao, X, LaFramboise, T, Giannoukos, G, Thomas, RK
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2005
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233602/ http://dx.doi.org/10.1186/bcr1181

Ejemplares similares

Evaluation of the arrayed primer extension resequencing assay for TP53 mutation detection
por: Due, EU, et al.
Publicado: (2005)

Single nucleotide polymorphism arrays: a decade of biological, computational and technological advances
por: LaFramboise, Thomas
Publicado: (2009)

Mutational spectrum of WTX, WT1, CTNNB1, APC and PLCG2 genes in Wilms tumor defined by massive parallel resequencing
por: Barros, Bruna D, et al.
Publicado: (2012)

Ciliome resequencing: A lifeline for molecular diagnosis in LCA
por: Perrault, I, et al.
Publicado: (2015)

Genome-wide SNP discovery from a pooled sample of accessions of the biofuel plant Jatropha curcas based on whole-transcriptome Illumina resequencing
por: Silva-Junior, Orzenil B, et al.
Publicado: (2011)

Gene discovery for motile cilia disorders: mutation spectrum in primary ciliary dyskinesia and discovery of mutations in CCDC151
por: Onoufriadis, A, et al.
Publicado: (2015)

An optimization framework for unsupervised identification of rare copy number variation from SNP array data
por: Yavaş, Gökhan, et al.
Publicado: (2009)

Observation of juvenile idiopathic arthritis in children with MEVF gene mutations in Armenia
por: Gayane, Khloyan, et al.
Publicado: (2008)

Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta
por: Wang, Yao, et al.
Publicado: (2015)

Correction: Development of a High-Throughput Resequencing Array for the Detection of Pathogenic Mutations in Osteogenesis Imperfecta
por: Wang, Yao, et al.
Publicado: (2015)

CytoConverter: a web-based tool to convert karyotypes to genomic coordinates
por: Wang, Janet, et al.
Publicado: (2019)

Resequencing Arrays for Diagnostics of Respiratory Pathogens
por: Lin, Baochuan, et al.
Publicado: (2009)

Allele-Specific Amplification in Cancer Revealed by SNP Array Analysis
por: LaFramboise, Thomas, et al.
Publicado: (2005)

Detection and quantification of mitochondrial DNA deletions from next-generation sequence data
por: Bosworth, Colleen M., et al.
Publicado: (2017)

The role of somatic NLRP3 mosaicism and new gene discovery in mutation negative cryopyrin-associated periodic syndrome patients
por: Gomes, Sonia Melo, et al.
Publicado: (2014)

Application of array comparative genomic hybridization (array- CGH) for detection of chromosomal imbalances in children with developmental delay/congenital malformations in Saudi Arabia
por: Hussein, Ibtessam Ramzi, et al.
Publicado: (2014)

Bead-based suspension array for detection and identification of tick-borne Borrelia species
por: Achterberg, RP, et al.
Publicado: (2014)

Two-view 2D digital mammography versus one-view digital breast tomosynthesis
por: Michell, MJ, et al.
Publicado: (2010)

Estimating the fraction of falsely detected spikes in high density microelectrode array recordings based on correlations
por: Muthmann, Jens-Oliver, et al.
Publicado: (2013)

Discovery of Gene Sources for Economic Traits in Hanwoo by Whole-genome Resequencing
por: Shin, Younhee, et al.
Publicado: (2016)

DB(2): a probabilistic approach for accurate detection of tandem duplication breakpoints using paired-end reads
por: Yavaş, Gökhan, et al.
Publicado: (2014)

Clinical phenotype and CARD15 gene mutation with Blau Syndrome in Chinese children and their parents
por: Li, C, et al.
Publicado: (2008)

Exome sequencing for disease gene discovery in Jeune’s Asphyxiating Thoracic Dystrophy
por: Taylor, P, et al.
Publicado: (2012)

A systematic strategy for the discovery of candidate genes responsible for phenotypic variation
por: Fisher, Paul, et al.
Publicado: (2007)

Evaluation of bacterial ribosomal RNA (rRNA) depletion methods for sequencing microbial community transcriptomes
por: Ciulla, Dawn, et al.
Publicado: (2010)

Unexpected cancer-predisposition gene variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome patients without underlying germline PTEN mutations
por: Yehia, Lamis, et al.
Publicado: (2018)

Variability of insulin sensitivity during the first 4 days of critical illness
por: Pretty, C, et al.
Publicado: (2012)

Accurate estimation of short read mapping quality for next-generation genome sequencing
por: Ruffalo, Matthew, et al.
Publicado: (2012)

Chromosomal imbalances mapped by array-based comparative genomic hybridization in an integrated approach to combat breast cancer in Denmark
por: Li, J, et al.
Publicado: (2005)

Chemokine and chemokine gene polymorphisms in exposed but uninfected partners of HIV-1 infected individuals in North India
por: Wanchu, A, et al.
Publicado: (2006)

Simulating electrode arrangements on microelectrode arrays
por: Vornanen, Inkeri, et al.
Publicado: (2015)

Discovery of a natural antagonist of macrophage migration inhibitory factor
por: Al-Abed, Y, et al.
Publicado: (2009)

Screening-mammography-detected lesions undergoing benign surgical excision: review of mammography features and preoperative needle biopsy results
por: Manuel, DD, et al.
Publicado: (2004)

Interplay between the innate immune response and heart rate variability in healthy human volunteers
por: Kox, M, et al.
Publicado: (2011)

Resequencing and Comparative Genomics of Stagonospora nodorum: Sectional Gene Absence and Effector Discovery
por: Syme, Robert Andrew, et al.
Publicado: (2013)

Mutations in the Fas gene found in Spanish ALPS (autoimmune lymphoproliferative syndrome) patients
por: Martínez-Martínez, L, et al.
Publicado: (2010)

Does tight glycemic control positively impact on patient mortality?
por: Penning, S, et al.
Publicado: (2012)

Validation of a virtual patient and virtual trials method for accurate prediction of tight glycemic control protocol performance
por: Suhaimi, F, et al.
Publicado: (2011)

Detection of low frequency variants of the NLRP3 gene in “mutation- negative” CAPS patients using massive parallel sequencing
por: Thiem, J, et al.
Publicado: (2015)

Modeling Extracellular Potentials in Microelectrode Array Recordings
por: Ness, Torbjørn B, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_sdjcg2gve8tpd8e7o7oafihngm