Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation - Wikidata - thesis-toulmin - TriplyDB

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

http://www.wikidata.org/entity/Q28207115

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Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence Genetics of autism spectrum disorder Allele quantification using molecular inversion probes (MIP).Genomic representations using concatenates of Type IIB restriction endonuclease digestion fragments Is NF-kappaB a good target for cancer therapy? Hopes and pitfalls Strong association of de novo copy number mutations with autism Identification and validation of oncogenes in liver cancer using an integrative oncogenomic approach Analysis of molecular inversion probe performance for allele copy number determination Oncogenic cooperation and coamplification of developmental transcription factor genes in lung cancer Application of array-based comparative genomic hybridization to clinical diagnostics Genetic alteration and gene expression modulation during cancer progression M-CGH: analysing microarray-based CGH experiments Gene expression profiling of epithelial ovarian tumours correlated with malignant potential SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data Allele-specific amplification in cancer revealed by SNP array analysis arrayCGHbase: an analysis platform for comparative genomic hybridization microarrays.CARAT: a novel method for allelic detection of DNA copy number changes using high density oligonucleotide arrays.BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH)Brk is coamplified with ErbB2 to promote proliferation in breast cancer Copy number polymorphism and expression level variation of the human alpha-defensin genes DEFA1 and DEFA3 Oncogenomics and the development of new cancer therapies An analytical pipeline for genomic representations used for cytosine methylation studies Tools for genomics Development of personalized tumor biomarkers using massively parallel sequencing DLC1 is a chromosome 8p tumor suppressor whose loss promotes hepatocellular carcinoma Identification and characterization of Dlc1 isoforms in the mouse and study of the biological function of a single gene trapped isoform Identification of tumor suppressors and oncogenes from genomic and epigenetic features in ovarian cancer Inferring tumor progression from genomic heterogeneity Reduced purifying selection prevails over positive selection in human copy number variant evolution Predicting cancer involvement of genes from heterogeneous data.Methylation detection oligonucleotide microarray analysis: a high-resolution method for detection of CpG island methylation.Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data.QuantiSNP: an Objective Bayes Hidden-Markov Model to detect and accurately map copy number variation using SNP genotyping data.Assessment of algorithms for high throughput detection of genomic copy number variation in oligonucleotide microarray data.Identification of cancer genes using a statistical framework for multiexperiment analysis of nondiscretized array CGH data.Genomic profiling by DNA amplification of laser capture microdissected tissues and array CGH Interrogation of genomes by molecular copy-number counting (MCC).Gene mutations and genomic rearrangements in the mouse as a result of transposon mobilization from chromosomal concatemers Using expression arrays for copy number detection: an example from E. coli Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.

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Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation

http://www.wikidata.org/entity/Q28207115

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2003 nî lūn-bûn

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2003 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2003 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2003年の論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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2003年論文

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Genome Research

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Adam Olshen

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Amy Brady

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Andrew Reiner

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Diane Esposito

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Ennapadam Venkatraman

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Jennifer Troge

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Joseph A West

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Ken C Q Nguyen

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P2860

Initial sequencing and analysis of the human genome

cDNA cloning and expression analysis of new members of the mammalian F-box protein family

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8

DBC2, a candidate for a tumor suppressor gene involved in breast cancer.

Gene expression profiling predicts clinical outcome of breast cancer

Normalization for cDNA microarray data: a robust composite method addressing single and multiple slide systematic variation.

PTEN, a putative protein tyrosine phosphatase gene mutated in human brain, breast, and prostate cancer

Molecular classification of cancer: class discovery and class prediction by gene expression monitoring

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

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2291-305

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scholarly article

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3074623

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10.1101/GR.1349003

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10

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13

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12975311

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403708

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