Cargando…

CNV-WebStore: Online CNV Analysis, Storage and Interpretation

BACKGROUND: Microarray technology allows the analysis of genomic aberrations at an ever increasing resolution, making functional interpretation of these vast amounts of data the main bottleneck in routine implementation of high resolution array platforms, and emphasising the need for a centralised a...

Descripción completa

Detalles Bibliográficos
Autores principales:	Vandeweyer, Geert, Reyniers, Edwin, Wuyts, Wim, Rooms, Liesbeth, Kooy, R Frank
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2011
Materias:	Software
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024943/ https://www.ncbi.nlm.nih.gov/pubmed/21208430 http://dx.doi.org/10.1186/1471-2105-12-4

Ejemplares similares

CNVassoc: Association analysis of CNV data using R
por: Subirana, Isaac, et al.
Publicado: (2011)

varAmpliCNV: analyzing variance of amplicons to detect CNVs in targeted NGS data
por: Kumar, Ajay Anand, et al.
Publicado: (2022)

X-CNV: genome-wide prediction of the pathogenicity of copy number variations
por: Zhang, Li, et al.
Publicado: (2021)

cnvCurator: an interactive visualization and editing tool for somatic copy number variations
por: Ma, Lingnan, et al.
Publicado: (2015)

Bayesian localization of CNV candidates in WGS data within minutes
por: Wiedenhoeft, John, et al.
Publicado: (2019)

SubPatCNV: approximate subspace pattern mining for mapping copy-number variations
por: Johnson, Nicholas, et al.
Publicado: (2015)

CNV Workshop: an integrated platform for high-throughput copy number variation discovery and clinical diagnostics
por: Gai, Xiaowu, et al.
Publicado: (2010)

MetaCNV - a consensus approach to infer accurate copy numbers from low coverage data
por: Friedrich, Stefanie, et al.
Publicado: (2020)

isoCNV: in silico optimization of copy number variant detection from targeted or exome sequencing data
por: Barcelona-Cabeza, Rosa, et al.
Publicado: (2021)

AutoCNV: a semiautomatic CNV interpretation system based on the 2019 ACMG/ClinGen Technical Standards for CNVs
por: Fan, Chunna, et al.
Publicado: (2021)

Gender differences in CNV burden do not confound schizophrenia CNV associations
por: Han, Jun, et al.
Publicado: (2016)

CNV-ClinViewer: enhancing the clinical interpretation of large copy-number variants online
por: Macnee, Marie, et al.
Publicado: (2023)

SavvyCNV: Genome-wide CNV calling from off-target reads
por: Laver, Thomas W., et al.
Publicado: (2022)

cnvScan: a CNV screening and annotation tool to improve the clinical utility of computational CNV prediction from exome sequencing data
por: Samarakoon, Pubudu Saneth, et al.
Publicado: (2016)

Reconstructing CNV genotypes using segregation analysis: combining pedigree information with CNV assay
por: Henshall, John M, et al.
Publicado: (2010)

Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients
por: Talseth-Palmer, Bente A, et al.
Publicado: (2013)

inCNV: An Integrated Analysis Tool for Copy Number Variation on Whole Exome Sequencing
por: Chanwigoon, Saowwapark, et al.
Publicado: (2020)

CNV analysis in the Lithuanian population
por: Urnikyte, A., et al.
Publicado: (2016)

Recurrent deletions of the X chromosome linked CNV64, CNV67, and CNV69 shows geographic differences across China and no association with idiopathic infertility in men
por: Ma, Xiulan, et al.
Publicado: (2017)

VariantDB: a flexible annotation and filtering portal for next generation sequencing data
por: Vandeweyer, Geert, et al.
Publicado: (2014)

affy2sv: an R package to pre-process Affymetrix CytoScan HD and 750K arrays for SNP, CNV, inversion and mosaicism calling
por: Hernandez-Ferrer, Carles, et al.
Publicado: (2015)

Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data
por: Kim, Soon-Young, et al.
Publicado: (2012)

Omics-informed CNV calls reduce false-positive rates and improve power for CNV-trait associations
por: Lepamets, Maarja, et al.
Publicado: (2022)

Copy number variation (CNV) identification, interpretation, and database from Brazilian patients
por: de Godoy, Victória Cabral Silveira Monteiro, et al.
Publicado: (2020)

CNV analysis of Meishan pig by next-generation sequencing and effects of AHR gene CNV on pig reproductive traits
por: Zheng, Xianrui, et al.
Publicado: (2020)

Immunosenescence in Choroidal Neovascularization (CNV)—Transcriptional Profiling of Naïve and CNV-Associated Retinal Myeloid Cells during Aging
por: Schlecht, Anja, et al.
Publicado: (2021)

The ICR96 exon CNV validation series: a resource for orthogonal assessment of exon CNV calling in NGS data
por: Mahamdallie, Shazia, et al.
Publicado: (2017)

Accuracy of CNV Detection from GWAS Data
por: Zhang, Dandan, et al.
Publicado: (2011)

Replicative mechanisms for CNV formation are error prone
por: Carvalho, Claudia M. B., et al.
Publicado: (2013)

PennCNV in whole-genome sequencing data
por: de Araújo Lima, Leandro, et al.
Publicado: (2017)

Common alleles contribute to schizophrenia in CNV carriers
por: Tansey, K E, et al.
Publicado: (2016)

CNV-Net: Segmentation, Classification and Activity Score Measurement of Choroidal Neovascularization (CNV) Using Optical Coherence Tomography Angiography (OCTA)
por: Vali, Mahsa, et al.
Publicado: (2023)

CNV comunicación no-verbal : cómo la inteligencia emocional se expresa a tráves de los gestos /
por: Rulicki, Sergio
Publicado: (2007)

Genome-wide algorithm for detecting CNV associations with diseases
por: Xu, Yaji, et al.
Publicado: (2011)

Whole-genome CNV analysis: advances in computational approaches
por: Pirooznia, Mehdi, et al.
Publicado: (2015)

Erratum: Common alleles contribute to schizophrenia in CNV carriers
por: Tansey, K E, et al.
Publicado: (2015)

Laser-induced CNV following hair removal procedure
por: Tofolean, Ioana Teodora, et al.
Publicado: (2019)

CNV Hotspots in Testicular Seminoma Tissue and Seminal Plasma
por: Raos, Dora, et al.
Publicado: (2021)

CNV-CH: A Convex Hull Based Segmentation Approach to Detect Copy Number Variations (CNV) Using Next-Generation Sequencing Data
por: Sinha, Rituparna, et al.
Publicado: (2015)

Treatment options for myopic CNV - Is photodynamic therapy still relevant?
por: Chew, Milton C, et al.
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_vdb484lh7gjogafa7hc5f6m1q5