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