array-cgh (Snijders Scientific)
90
Structured Review
Snijders Scientific
array-cgh
Array Cgh, supplied by Snijders Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high-throughput+microarray-based+assays+infinium+platform/array+cgh/pmc01872007-114-0-31
Average 90 stars, based on 1 article reviews
Array Cgh, supplied by Snijders Scientific, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/high-throughput+microarray-based+assays+infinium+platform/array+cgh/pmc01872007-114-0-31
Average 90 stars, based on 1 article reviews
array-cgh - by Bioz Stars,
2026-11
90/100 stars
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Labeling:Article Title: Stromal control of oncogenic traits expressed in response to overexpression of GLI2 , a pleiotropic oncogene Article Snippet: .. Labeling of DNA for Hybridization:Article Title: Stromal control of oncogenic traits expressed in response to overexpression of GLI2 , a pleiotropic oncogene Article Snippet: .. Labeling of DNA for Article Title: SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control. Article Snippet: Array-based comparative genomic hybridization analysis of genomic DNA was first applied in postnatal diagnosis for patients with intellectual disability (ID) and/or congenital anomalies (CA).. Genome-wide single-nucleotide polymorphism (SNP) array analysis was subsequently implemented as the first line diagnostic test for ID/CA patients in our laboratory in 2009, because its diagnostic yield is significantly higher than that of routine cytogenetic analysis.. In addition to the detection of copy number variations, the genotype information obtained with SNP array analysis enables the detection of stretches of homozygosity and thereby the possible identification of recessive disease genes, mosaic aneuploidy, or uniparental disomy. Genome Wide:Article Title: SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control. Article Snippet: Array-based comparative genomic hybridization analysis of genomic DNA was first applied in postnatal diagnosis for patients with intellectual disability (ID) and/or congenital anomalies (CA).. Genome-wide single-nucleotide polymorphism (SNP) array analysis was subsequently implemented as the first line diagnostic test for ID/CA patients in our laboratory in 2009, because its diagnostic yield is significantly higher than that of routine cytogenetic analysis.. In addition to the detection of copy number variations, the genotype information obtained with SNP array analysis enables the detection of stretches of homozygosity and thereby the possible identification of recessive disease genes, mosaic aneuploidy, or uniparental disomy. BAC Assay:Article Title: Technology-driven and evidence-based genomic analysis for integrated pediatric and prenatal genetics evaluation. Article Snippet: The first decade since the completion of the Human Genome Project has been marked with rapid development of genomic technologies and their immediate clinical applications.. Genomic analysis using oligonucleotide array comparative genomic hybridization (aCGH) or single nucleotide polymorphism (SNP) chips has been applied to pediatric patients with developmental and intellectual disabilities (DD/ ID), multiple congenital anomalies (MCA) and autistic spectrum disorders (ASD).. Evaluation of analytical and clinical validities of aCGH showed > 99% sensitivity and specificity and increased analytical resolution by higher density probe coverage. Article Title: Methods for nucleic acid mapping and identification of fine-structural-variations in nucleic acids Article Snippet: .. Clone Assay:Article Title: Technology-driven and evidence-based genomic analysis for integrated pediatric and prenatal genetics evaluation. Article Snippet: The first decade since the completion of the Human Genome Project has been marked with rapid development of genomic technologies and their immediate clinical applications.. Genomic analysis using oligonucleotide array comparative genomic hybridization (aCGH) or single nucleotide polymorphism (SNP) chips has been applied to pediatric patients with developmental and intellectual disabilities (DD/ ID), multiple congenital anomalies (MCA) and autistic spectrum disorders (ASD).. Evaluation of analytical and clinical validities of aCGH showed > 99% sensitivity and specificity and increased analytical resolution by higher density probe coverage. Article Title: Biomarkers for prostate cancer metastasis Article Snippet: .. To identify the gained and lost clones in individual samples, we constructed sample-specific thresholds (Fridlyand, J., Snijders, A., Pinkel, D., Albertson, D. G. and Jain, A. N. (2004) Application of Hidden Markov Models to the analysis of the Produced:Article Title: Technology-driven and evidence-based genomic analysis for integrated pediatric and prenatal genetics evaluation. Article Snippet: The first decade since the completion of the Human Genome Project has been marked with rapid development of genomic technologies and their immediate clinical applications.. 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Kestler, Wolfram Klapper, Markus Kreuz, Dido Lenze, Markus Loeffler, Peter Möller, Hans-Konrad Müller-Hermelink, German Ott, Maciej Rosolowski, Andreas Rosenwald, Sandra Ruf, Reiner Siebert, Rainer Spang, Harald Stein, Lorenz Truemper, Peter Lichter, Martin Bentz, and Swen Wessendorf; for the Molecular Mechanisms in Malignant Lymphomas Network Project of the Deutsche Krebshilfe Abt.Innere Medizin III,Zentrumfˇr Innere Medizin der Universit t Ulm,Robert-Koch-Str.8,D-89081Ulm,Germany Institut fˇrmedizinische Informtik,Statistikund Epidemiologie,Universit t Leipzig,H rtelstrabe16-18,D-04107 Leipzig,Germany Abt.Pathologie,Universit t Ulm,Albert-Einstein-Allee11,D-89081Ulm,Germany Institut fˇr Funktionale Genomik,Universit t Regensburg,Josef-Engert-Str.9,D-93053 Regensburg,Germany Institut fˇr Pathologie,Universit tsklinik Schleswig-Holstein,Campus Lˇbeck,Ratzeburger Allee160,D-23538 Lˇbeck,Germany Institut fˇr Pathologie,Universit tsklinik Frankfurt,Theodor-Stern-Kai 7,D-60590 Frankfurt amMain,Germany InstitutfˇrPathologie,CampusBenjaminFranklin,Charite¤ -Universit tsmedizinBerlin,Hindenburgdamm30,D-12200Berlin,Germany Forschungsdozentur Bioinformatik,Universit t Ulm,Robert-Koch Strasse 8,D-89081Ulm,Germany Pathologie Kiel,Institut fˇr H matopathologie und Lymphknotenregister Kiel,Universit tsklinikum Schleswig-Holstein,Campus Kiel, Niemannsweg11,D-24105 Kiel,Germany Institut fˇr Pathologie,Universit tWˇrzburg,Josef-Schneider-Str.. 2,D-97080Wˇrzburg,Germany Institut fˇrklinische Pathologie,Robert-Bosch-Krankenhaus,Auerbachstrabe110,D-70376 Stuttgart,Germany Institut fˇr Humangenetik,Universit tsklinikum Schleswig-Holstein,Campus Kiel, Schwanenweg 24,D-24105 Kiel,Germany Abt. fˇr H matologie und Onkologie,Georg-August Universit t G ̨ttingen,Robert-Koch-Str.40,D-37075 G ̨ttingen,Germany Abt.Molekulare Genetik,Deutsches Krebsforschungszentrum,ImNeuenheimer Feld 280,D-69120 Heidelberg,Germany Medizinische Klinik II, St dtisches Klinikum Karlsruhe,Moltkestrasse 90,D-76133 Karlsruhe,Germany |