نتایج جستجو برای: comparative genomic hybridization

تعداد نتایج: 397000  

Journal: :Cancer research 2002
Véronique Bourdon Félix Naef Pulivarthi H Rao Victor Reuter Samuel C Mok George J Bosl Sanjay Koul Vundaralli V V S Murty Raju S Kucherlapati R S K Chaganti

We performed parallel array comparative genomic hybridization and array expression analysis of the 12p11-p12 amplicon in human testicular seminomas and an ovarian carcinoma cell line using an expressed sequence tags (ESTs) array spotted with 8254 ESTs. The data were normalized using a robust statistical modeling and the significance inferred from the local SD. We identified two ESTs within the ...

2013
Siddharth Roy Alison Motsinger Reif

Copy number variation (CNV) detection has become an integral part many of genetic studies and new technologies promise to revolutionize our ability to detect and link them to disease. However, recent studies highlight discrepancies in the genome wide CNV profile when measured by different technologies and even by the same technology. Furthermore, the change point algorithms used to call CNVs ca...

Journal: :Prenatal diagnosis 2014
Angelique J A Kooper Brigitte H W Faas

NE Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK TDL Genetics, The Doctors Laboratory, London, UK UCL Institute of Child Health, London, UK University College Hospital NHS Foundation Trust, London, UK Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK *Correspondence to: Lyn S. Chitty. E-mail: [email protected]...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2001
A N Jain K Chin A L Børresen-Dale B K Erikstein P Eynstein Lonning R Kaaresen J W Gray

We present a general method for rigorously identifying correlations between variations in large-scale molecular profiles and outcomes and apply it to chromosomal comparative genomic hybridization data from a set of 52 breast tumors. We identify two loci where copy number abnormalities are correlated with poor survival outcome (gain at 8q24 and loss at 9q13). We also identify a relationship betw...

Journal: :Clinical genetics 2012
A L Mosca-Boidron S Bouquillon L Faivre P Callier J Andrieux N Marle C Bonnet C Vincent-Delorme M Berri G Plessis S Manouvrier-Hanu A Dieux-Coeslier C Thauvin-Robinet E Pipiras A Delahaye M Payet C Ragon A Masurel-Paulet E Questiaux B Benzacken P Jonveaux F Mugneret M Holder-Espinasse

Most microdeletion syndromes identified before the implementation of array-comparative genomic hybridization (array-CGH) were presumed to be well-defined clinical entities. However, the introduction of whole-genome screening led not only to the description of new syndromes but also to the recognition of a broader spectrum of features for well-known syndromes. Here, we report on 10 patients pres...

2012
Sergio E Cury

The safe distinction between benign and malignant pheochromocytomas is still an unsolved problem from the standpoint of the pathological diagnosis. In most cases, the decision is thus based on the occurrence of metastasis as the only unambiguous evidence of malignancy. This paper reviews the literature and shows that, although there are positive correlations between anatomopathological, immunoh...

2008
Robert G. Clark Y.-X. Lin V. Baladandayuthapani V. Bonato

Motivation: Existing methods for estimating copy number variations in array comparative genomic hybridization (aCGH) data are limited to estimations of the gain/loss of chromosome regions for single sample analysis. We propose the linear-median method for estimating shared copy numbers in DNA sequences across multiple samples, demonstrate its operating characteristics through simulations and ap...

2010
Avigail Agam Binnaz Yalcin Amarjit Bhomra Matthew Cubin Caleb Webber Christopher Holmes Jonathan Flint Richard Mott

BACKGROUND Array comparative genomic hybridization (aCGH) to detect copy number variants (CNVs) in mammalian genomes has led to a growing awareness of the potential importance of this category of sequence variation as a cause of phenotypic variation. Yet there are large discrepancies between studies, so that the extent of the genome affected by CNVs is unknown. We combined molecular and aCGH an...

Journal: :Haematologica 2008
Fabrice Jardin Philippe Ruminy Jean-Pierre Kerckaert Françoise Parmentier Jean-Michel Picquenot Sabine Quief Céline Villenet Gérard Buchonnet Mario Tosi Thierry Frebourg Christian Bastard Hervé Tilly

BACKGROUND Genomic gains and losses play a crucial role in the development of diffuse large B-cell lymphomas. High resolution array comparative genomic hybridization provides a comprehensive view of these genomic imbalances but is not routinely applicable. We developed a polymerase chain reaction assay to provide information regarding gains or losses of relevant genes and prognosis in diffuse l...

Journal: :BioTechniques 2008
Lars Prestegarden Anjan Misra Marcus L Ware Ru-Fang Yeh Rolf Bjerkvig Burt G Feuerstein

Array comparative genomic hybridization (aCGH) is a powerful tool to detect relative DNA copy number at a resolution limited only by the coverage of bacterial artificial chromosomes (BACs) used to print the genomic array. The amount of DNA needed to perform a reliable aCGH analysis has been a limiting factor, especially on minute tissue samples where limited DNA is available. Here we report a s...

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