High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays. - Wikidata - awgldk - TriplyDB

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

http://www.wikidata.org/entity/Q24545276

about

Getting started in tiling microarray analysis Personal genome sequencing: current approaches and challenges Paired-end mapping reveals extensive structural variation in the human genome Mapping of transcription factor binding regions in mammalian cells by ChIP: comparison of array- and sequencing-based technologies The Danish 22q11 research initiative PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data The 22q11.2 microdeletion: fifteen years of insights into the genetic and neural complexity of psychiatric disorders.22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia.Flexible and accurate detection of genomic copy-number changes from aCGH.Validation of rearrangement break points identified by paired-end sequencing in natural populations of Drosophila melanogaster.Parametric modeling of whole-genome sequencing data for CNV identification.QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.Tilescope: online analysis pipeline for high-density tiling microarray data.ADaCGH: A parallelized web-based application and R package for the analysis of aCGH data.High-resolution copy-number variation map reflects human olfactory receptor diversity and evolution.Mismatch oligonucleotides in human and yeast: guidelines for probe design on tiling microarrays.A deletion and a duplication in distal 22q11.2 deletion syndrome region. Clinical implications and review TileProbe: modeling tiling array probe effects using publicly available data Integrating sequencing technologies in personal genomics: optimal low cost reconstruction of structural variants Molecular mechanisms and diagnosis of chromosome 22q11.2 rearrangements Deletion Extents Are Not the Cause of Clinical Variability in 22q11.2 Deletion Syndrome: Does the Interaction between DGCR8 and miRNA-CNVs Play a Major Role?A robust penalized method for the analysis of noisy DNA copy number data.Detection of copy number variation from array intensity and sequencing read depth using a stepwise Bayesian model.Systematic inference of copy-number genotypes from personal genome sequencing data reveals extensive olfactory receptor gene content diversity Identification of genes and genomic islands correlated with high pathogenicity in Streptococcus suis using whole genome tiling microarrays.Identification of genomic indels and structural variations using split reads Behavior, brain, and genome in genomic disorders: finding the correspondences.Quality of Cell Products: Authenticity, Identity, Genomic Stability and Status of Differentiation.Common copy number variation detection from multiple sequenced samples Phenotypic impact of genomic structural variation: insights from and for human disease.Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11 Genotype-phenotype correlation in 22q11.2 deletion syndrome.Robust Detection and Identification of Sparse Segments in Ultra-High Dimensional Data Analysis.The current excitement about copy-number variation: how it relates to gene duplications and protein families.BreakDancer: an algorithm for high-resolution mapping of genomic structural variation.Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV Tetralogy of Fallot and Hypoplastic Left Heart Syndrome - Complex Clinical Phenotypes Meet Complex Genetic Networks Transcriptome Profiling of Peripheral Blood in 22q11.2 Deletion Syndrome Reveals Functional Pathways Related to Psychosis and Autism Spectrum Disorder

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High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

http://www.wikidata.org/entity/Q24545276

description

2006 nî lūn-bûn

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2006 թուականի Մարտին հրատարակուած գիտական յօդուած

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2006 թվականի մարտին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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Proceedings of the National Academy of Sciences of the United States of America

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High-resolution mapping of DNA ...... tiling oligonucleotide arrays.

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Alexander Eckehart Urban

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April Hacker

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Beverly S Emanuel

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George V Popescu

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Joseph F Cubells

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Michael Snyder

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Rebecca Selzer

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Roland Green

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Sherman M Weissman

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Todd Richmond

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P2860

Fine-scale structural variation of the human genome

Initial sequence of the chimpanzee genome and comparison with the human genome

Genomic disorders on 22q11

Gene expression analysis using oligonucleotide arrays produced by maskless photolithography

Recent segmental and gene duplications in the mouse genome

A new non-linear normalization method for reducing variability in DNA microarray experiments.

Detection of large-scale variation in the human genome

Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

Chromosomal microdeletions: dissecting del22q11 syndrome

Segmental duplications and copy-number variation in the human genome.

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4534-4539

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10.1073/PNAS.0511340103

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12

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103

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Mark Bender Gerstein

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2006-03-14T00:00:00Z

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7241955

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1450206

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