A comprehensive analysis of common copy-number variations in the human genome. - Wikidata - awgldk - TriplyDB

A comprehensive analysis of common copy-number variations in the human genome.

A comprehensive analysis of common copy-number variations in the human genome.

http://www.wikidata.org/entity/Q35616521

about

Mechanisms of change in gene copy number Mapping and sequencing of structural variation from eight human genomes A diverse array of genetic factors contribute to the pathogenesis of systemic lupus erythematosus Ultraconserved elements: analyses of dosage sensitivity, motifs and boundaries Disruption of the neurexin 1 gene is associated with schizophrenia High resolution genomic analysis of 18q- using oligo-microarray comparative genomic hybridization (aCGH)Detailed analysis of 22q11.2 with a high density MLPA probe set Ohno's dilemma: evolution of new genes under continuous selection Statistical analysis for genome-wide association study Microarray resources for genetic and genomic studies in chicken: a review Autism: the quest for the genes Cole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HB Three tiers of genome evolution in reptiles Reduced purifying selection prevails over positive selection in human copy number variant evolution Massive screening of copy number population-scale variation in Bos taurus genome PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Genotype-phenotype relationship in three cases with overlapping 19p13.12 microdeletions.Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.Genetic disruption of KEAP1/CUL3 E3 ubiquitin ligase complex components is a key mechanism of NF-kappaB pathway activation in lung cancer.Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.Classifying the Progression of Ductal Carcinoma from Single-Cell Sampled Data via Integer Linear Programming: A Case Study.Gene expression profile analysis of pancreatic cancer based on microarray data.QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.Pharmacogenetics: data, concepts and tools to improve drug discovery and drug treatment.wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data MD-SeeGH: a platform for integrative analysis of multi-dimensional genomic data.Large-scale copy number variants (CNVs): distribution in normal subjects and FISH/real-time qPCR analysis.Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.X-chromosome tiling path array detection of copy number variants in patients with chromosome X-linked mental retardation.Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility Improved detection of global copy number variation using high density, non-polymorphic oligonucleotide probes Probe-specific mixed-model approach to detect copy number differences using multiplex ligation-dependent probe amplification (MLPA).Mathematical analysis of copy number variation in a DNA sample using digital PCR on a nanofluidic device Small deletion variants have stable breakpoints commonly associated with alu elements.Copy number variations (CNVs) identified in Korean individuals.A snapshot of CNVs in the pig genome Quantitative analysis of single nucleotide polymorphisms within copy number variation Chromosomal minimal critical regions in therapy-related leukemia appear different from those of de novo leukemia by high-resolution aCGH.A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan

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P2860

A comprehensive analysis of common copy-number variations in the human genome.

http://www.wikidata.org/entity/Q35616521

description

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2006年论文

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name

A comprehensive analysis of common copy-number variations in the human genome.

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A comprehensive analysis of common copy-number variations in the human genome.

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type

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A comprehensive analysis of common copy-number variations in the human genome.

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A comprehensive analysis of common copy-number variations in the human genome.

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A comprehensive analysis of common copy-number variations in the human genome.

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A comprehensive analysis of common copy-number variations in the human genome.

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American Journal of Human Genetics

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A comprehensive analysis of common copy-number variations in the human genome.

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Douglas E Horsman

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Evan E Eichler

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Kendy K Wong

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Lindsey R Kimm

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Nirpjit S Dosanjh

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Raymond T Ng

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Ronald J deLeeuw

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Wan L Lam

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Ze Cheng

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P2860

Fine-scale structural variation of the human genome

Finishing the euchromatic sequence of the human genome

The microRNA Registry

Cluster analysis and display of genome-wide expression patterns

A haplotype map of the human genome

SeeGH--a software tool for visualization of whole genome array comparative genomic hybridization data

A stepwise framework for the normalization of array CGH data.

A method for accurate detection of genomic microdeletions using real-time quantitative PCR.

Primer3 on the WWW for general users and for biologist programmers

MicroRNAs: genomics, biogenesis, mechanism, and function

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