Literature DB >> 21536241

Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula.

Roberto Valli1, Emanuela Maserati, Cristina Marletta, Barbara Pressato, Francesco Lo Curto, Francesco Pasquali.   

Abstract

Array-based comparative genomic hybridization (aCGH) has proven indispensable to the study of unbalanced constitutional and acquired chromosomal anomalies, but its sensitivity for detecting mosaicism is still not well established. On the basis of the ADM2 algorithm used for microarray image analysis with one of the most widely used oligomer-based aCGH platforms [the whole genome 244K system by Agilent Technologies (Santa Clara, CA)] we suggest a formula to infer the percentage of cells bearing a chromosome imbalance in cases with constitutional or acquired mosaicism. Three examples of acquired mosaicism in which this formula was applied are reported together with parallel fluorescence in situ hybridization (FISH) to interphase nuclei with informative probes. Although some approximation affects both the results inferred from aCGH and FISH data, the proposed formula was successful in the three patients studied.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21536241     DOI: 10.1016/j.cancergen.2011.02.002

Source DB:  PubMed          Journal:  Cancer Genet


  8 in total

1.  Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells.

Authors:  Roberto Valli; Cristina Marletta; Barbara Pressato; Giuseppe Montalbano; Francesco Lo Curto; Francesco Pasquali; Emanuela Maserati
Journal:  Mol Cytogenet       Date:  2011-05-09       Impact factor: 2.009

2.  Functional in vivo and in vitro effects of 20q11.21 genetic aberrations on hPSC differentiation.

Authors:  Hye-Yeong Jo; Youngsun Lee; Hongryul Ahn; Hyeong-Jun Han; Ara Kwon; Bo-Young Kim; Hye-Yeong Ha; Sang Cheol Kim; Jung-Hyun Kim; Yong-Ou Kim; Sun Kim; Soo Kyung Koo; Mi-Hyun Park
Journal:  Sci Rep       Date:  2020-10-29       Impact factor: 4.379

3.  Different loss of material in recurrent chromosome 20 interstitial deletions in Shwachman-Diamond syndrome and in myeloid neoplasms.

Authors:  Roberto Valli; Barbara Pressato; Cristina Marletta; Lydia Mare; Giuseppe Montalbano; Francesco Lo Curto; Francesco Pasquali; Emanuela Maserati
Journal:  Mol Cytogenet       Date:  2013-12-12       Impact factor: 2.009

4.  Genome-wide screening of cytogenetic abnormalities in multiple myeloma patients using array-CGH technique: a Czech multicenter experience.

Authors:  Jan Smetana; Jan Frohlich; Romana Zaoralova; Vladimira Vallova; Henrieta Greslikova; Renata Kupska; Pavel Nemec; Aneta Mikulasova; Martina Almasi; Ludek Pour; Zdenek Adam; Viera Sandecka; Lenka Zahradová; Roman Hajek; Petr Kuglik
Journal:  Biomed Res Int       Date:  2014-06-02       Impact factor: 3.411

5.  Gene expression profile of glioblastoma peritumoral tissue: an ex vivo study.

Authors:  Annunziato Mangiola; Nathalie Saulnier; Pasquale De Bonis; Daniela Orteschi; Gigliola Sica; Gina Lama; Benedetta Ludovica Pettorini; Giovanni Sabatino; Marcella Zollino; Libero Lauriola; Anna Colabianchi; Gabriella Proietti; Gyula Kovacs; Giulio Maira; Carmelo Anile
Journal:  PLoS One       Date:  2013-03-05       Impact factor: 3.240

6.  A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature.

Authors:  Pavel Tesner; Jana Drabova; Miroslav Stolfa; Martin Kudr; Martin Kyncl; Veronika Moslerova; Drahuse Novotna; Radka Kremlikova Pourova; Eduard Kocarek; Tereza Rasplickova; Zdenek Sedlacek; Marketa Vlckova
Journal:  Mol Cytogenet       Date:  2018-05-09       Impact factor: 2.009

7.  Microarray expression studies on bone marrow of patients with Shwachman-Diamond syndrome in relation to deletion of the long arm of chromosome 20, other chromosome anomalies or normal karyotype.

Authors:  Abdul Waheed Khan; Antonella Minelli; Annalisa Frattini; Giuseppe Montalbano; Alessia Bogni; Marco Fabbri; Giovanni Porta; Francesco Acquati; Rita Maria Pinto; Elena Bergami; Rossella Mura; Anna Pegoraro; Simone Cesaro; Marco Cipolli; Marco Zecca; Cesare Danesino; Franco Locatelli; Emanuela Maserati; Francesco Pasquali; Roberto Valli
Journal:  Mol Cytogenet       Date:  2020-01-02       Impact factor: 2.009

8.  Mosaic complete tetrasomy 21 in a fetus with complete atrioventricular septal defect and minor morphological variations.

Authors:  Vincent Gatinois; Nicole Bigi; Eve Mousty; Jean Chiesa; Yuri Musizzano; Anouck Schneider; Geneviève Lefort; Lucile Pinson; Jean-Baptiste Gaillard; Clémence Ragon; Marie-Josée Perez; Magali Tournaire; Patricia Blanchet; Carole Corsini; Emmanuelle Haquet; Patrick Callier; David Geneviève; Franck Pellestor; Jacques Puechberty
Journal:  Mol Genet Genomic Med       Date:  2019-09-07       Impact factor: 2.183

  8 in total

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