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Li-fraumeni syndromeComputational methods for detecting copy number variations in cancer genome using next generation sequencing: principles and challengesConnecting Anxiety and Genomic Copy Number Variation: A Genome-Wide Analysis in CD-1 MiceComparative analysis of copy number variation detection methods and database constructionEvaluation of somatic copy number estimation tools for whole-exome sequencing data.cisASE: a likelihood-based method for detecting putative cis-regulated allele-specific expression in RNA sequencing data.How old are you? Genet age estimates in a clonal animal.HYSYS: have you swapped your samples?Gene-based comparative analysis of tools for estimating copy number alterations using whole-exome sequencing data.Prediction of years of life after diagnosis of breast cancer using omics and omic-by-treatment interactions.An evaluation of copy number variation detection tools for cancer using whole exome sequencing data.Assessment of circulating copy number variant detection for cancer screening.Impact on disease development, genomic location and biological function of copy number alterations in non-small cell lung cancer.Application of OMICS technologies in occupational and environmental health research; current status and projections.ClipCrop: a tool for detecting structural variations with single-base resolution using soft-clipping informationVCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism.Similarity-based methods for potential human microRNA-disease association predictionCopy number variation analysis by ligation-dependent PCR based on magnetic nanoparticles and chemiluminescence.Copy number variation analysis based on AluScan sequencesLarge-scale integrative network-based analysis identifies common pathways disrupted by copy number alterations across cancers.Copy number variations are progressively associated with the pathogenesis of colorectal cancer in ulcerative colitisSubPatCNV: approximate subspace pattern mining for mapping copy-number variationsIdentification of rare germline copy number variations over-represented in five human cancer types.Influence of aflatoxin B1 on copy number variants in human leukocytes in vitroXomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.miR-24-2 controls H2AFX expression regardless of gene copy number alteration and induces apoptosis by targeting antiapoptotic gene BCL-2: a potential for therapeutic intervention.SCNVSim: somatic copy number variation and structure variation simulatorcnvCurator: an interactive visualization and editing tool for somatic copy number variations.Penalized weighted low-rank approximation for robust recovery of recurrent copy number variations.An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.Comparative analysis of copy number variations in ulcerative colitis associated and sporadic colorectal neoplasia.Comparison of microfluidic digital PCR and conventional quantitative PCR for measuring copy number variation.Representing and decomposing genomic structural variants as balanced integer flows on sequence graphs.Analysis of gene copy number changes in tumor phylogeneticsCo-clustering phenome-genome for phenotype classification and disease gene discovery.Genome-wide identification of copy number variations in Chinese Holstein.Inherited susceptibility to chronic lymphocytic leukemia: evidence and prospects for the future.The clinical context of copy number variation in the human genome.Identifying the clonal origin of synchronous multifocal tumors in the hepatobiliary and pancreatic system using multi-omic platforms.Genome-based versus gene-based theory of cancer: possible implications for clinical practice.
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P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 16 June 2009
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Copy number variations and cancer.
@en
Copy number variations and cancer.
@nl
type
label
Copy number variations and cancer.
@en
Copy number variations and cancer.
@nl
prefLabel
Copy number variations and cancer.
@en
Copy number variations and cancer.
@nl
P2860
P356
P1433
P1476
Copy number variations and cancer.
@en
P2093
Adam Shlien
P2860
P2888
P356
10.1186/GM62
P50
P577
2009-06-16T00:00:00Z
P5875
P6179
1002911260