1 |
array comparative genomic hybridization
(1506 times)
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Neoplasms (306 times)
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FISH (248 times) CNVs (137 times) MLPA (76 times)
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2003 1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis.
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2 |
array CGH
(43 times)
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Neoplasms (12 times)
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CNVs (7 times) FISH (3 times) ID (3 times)
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2003 Combined array comparative genomic hybridization and tissue microarray analysis suggest PAK1 at 11q13.5-q14 as a critical oncogene target in ovarian carcinoma.
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3 |
array-based CGH
(6 times)
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Neoplasms (5 times)
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CGH (2 times) HCC (2 times) CNVs (1 time)
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2007 Genomic analysis of CD8+ NK/T cell line, 'SRIK-NKL', with array-based CGH (aCGH), SKY/FISH and molecular mapping.
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4 |
authors conducted microarray-based comparative genomic hybridization
(5 times)
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Molecular Biology (1 time)
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FISH (2 times) SNP (2 times) DLRSpread (1 time)
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2009 Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.
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5 |
arrayCGH
(2 times)
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Biomedical Research (1 time)
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cfDNA (1 time) MNA (1 time) NCA (1 time)
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2014 Mapping of the chromosomal amplification 1p21-22 in bladder cancer.
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6 |
aberrations in these cells with the microarray-based comparative genomic hybridization
(1 time)
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Biomedical Research (1 time)
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PMA (1 time)
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2009 High-resolution analysis of aberrant regions in autosomal chromosomes in human leukemia THP-1 cell line.
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7 |
address this question, we utilized microarray comparative genomic hybridization
(1 time)
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Pathology (1 time)
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2014 Comparative genomic hybridization in a case of melanoma that loses expression of S100, HMB45, Melan A and tyrosinase in metastasis.
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8 |
adults with ALL by whole-genome oligonucleotide array
(1 time)
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Medicine (1 time)
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ALL (1 time) CNAs (1 time) OS (1 time)
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2016 Genome-Wide DNA Copy Number Analysis of Acute Lymphoblastic Leukemia Identifies New Genetic Markers Associated with Clinical Outcome.
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9 |
aims to describe how microarray comparative genomic hybridization
(1 time)
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Gynecology (1 time)
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2017 Prenatal microarray comparative genomic hybridization: Experience from the two first years of activity at the Lyon university-hospital.
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10 |
Alterations in Single Cells Using Microarray-Based Comparative Genomic Hybridization
(1 time)
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Cell Biology (1 time)
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PBMC (1 time)
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2014 Analysis of Copy-Number Alterations in Single Cells Using Microarray-Based Comparative Genomic Hybridization (aCGH).
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11 |
ambiguous results from microarray-based comparative genomic hybridization
(1 time)
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Genetics (1 time)
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CNVs (1 time) qPCR (1 time)
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2009 Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.
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12 |
amplification identified by microarray-based comparative genomic hybridization
(1 time)
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Clinical Laboratory Techniques (1 time)
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BACs (1 time) CCND1 (1 time) FFPETS (1 time)
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2006 Unlocking pathology archives for molecular genetic studies: a reliable method to generate probes for chromogenic and fluorescent in situ hybridization.
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13 |
amplification method, followed by either comparative genome hybridization
(1 time)
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Molecular Biology (1 time)
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2015 Copy Number Variation Analysis by Array Analysis of Single Cells Following Whole Genome Amplification.
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14 |
analysed with high resolution, microarray-based, comparative genomic hybridisation
(1 time)
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Genetics, Medical (1 time)
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FFPE (1 time) HCC (1 time)
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2016 Distinct set of chromosomal aberrations in childhood hepatocellular carcinoma is correlated to hepatitis B virus infection.
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15 |
analysis based on Comparative Genomic Hybridization
(1 time)
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Cytogenetics (1 time)
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CMA (1 time) FISH (1 time) idicY (1 time)
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2019 Discrepancy of QF-PCR, CMA and karyotyping on a de novo case of mosaic isodicentric Y chromosomes.
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16 |
analyzed by oligonucleotide microarray comparative genomic hybridization
(1 time)
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Cytogenetics (1 time)
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AML (1 time) FISH (1 time) OS (1 time)
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2015 Double inv(3)(q21q26.2) in acute myeloid leukemia is resulted from an acquired copy neutral loss of heterozygosity of chromosome 3q and associated with disease progression.
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17 |
analyzed for their chromosome complement using microarray comparative genomic hybridization
(1 time)
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Reproductive Medicine (1 time)
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NIHR (1 time)
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2017 The incidence and origin of segmental aneuploidy in human oocytes and preimplantation embryos.
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18 |
applied, ranging from the conventional cytogenetic analysis, through microarray-based methods
(1 time)
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CNVs (1 time) kb (1 time) NGS (1 time)
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2021 Copy Number Variant Detection with Low-Coverage Whole-Genome Sequencing Represents a Viable Alternative to the Conventional Array-CGH.
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19 |
array collection for comparative genomic hybridisation
(1 time)
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Neoplasms (1 time)
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BAC (1 time)
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2009 A high-resolution integrated analysis of genetic and expression profiles of breast cancer cell lines.
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20 |
Array comparative genomic hybrid
(1 time)
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Endocrinology (1 time)
|
GH (1 time) IGF-1 (1 time) PRL (1 time)
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2020 A Chinese Case of X-Linked Acrogigantism and Systematic Review.
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21 |
array for CGH
(1 time)
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Neoplasms (1 time)
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CNV (1 time) HBOC (1 time) NGS (1 time)
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2016 Ready to clone: CNV detection and breakpoint fine-mapping in breast and ovarian cancer susceptibility genes by high-resolution array CGH.
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22 |
array-based CGH analysis
(1 time)
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Ophthalmology (1 time)
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MLPA (1 time) USH1F (1 time)
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2010 Identification of large rearrangements of the PCDH15 gene by combined MLPA and a CGH: large duplications are responsible for Usher syndrome.
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23 |
array-based genomic hybridization
(1 time)
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Neoplasms (1 time)
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UC (1 time)
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2015 CEBPD amplification and overexpression in urothelial carcinoma: a driver of tumor metastasis indicating adverse prognosis.
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24 |
artificial chromosome microarray comparative genomic hybridisation
(1 time)
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Clinical Laboratory Techniques (1 time)
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2006 Evaluation of Phi29-based whole-genome amplification for microarray-based comparative genomic hybridisation.
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25 |
CGH and microarray-CGH
(1 time)
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Reproductive Medicine (1 time)
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CGH (1 time) FISH (1 time) TE (1 time)
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2010 Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation.
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26 |
cytogenetics and comparative genomic hybridization
(1 time)
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Neoplasms (1 time)
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EGFR (1 time) PN (1 time)
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2018 High level EGFR amplification in a newly established glioblastoma cell line 170-MG-BA.
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27 |
HER2-amplified cancers using tiling path microarray-based comparative genomic hybridization
(1 time)
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Pathology (1 time)
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2008 The genomic profile of HER2-amplified breast cancers: the influence of ER status.
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28 |
oligonucleotide-based comparative genomic hybridization arrays
(1 time)
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Genetics, Medical (1 time)
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DUSP22 (1 time) FOX (1 time) SNP (1 time)
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2011 A complex 6p25 rearrangement in a child with multiple epiphyseal dysplasia.
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