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Abbreviation: aCGH
Appearance Frequency: 1349 time(s)
Long forms: 26

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
array comparative genomic hybridization
(1277 times)
Neoplasms
(287 times)
FISH (187 times)
CNVs (114 times)
MLPA (58 times)
2004 1-Mb resolution array-based comparative genomic hybridization using a BAC clone set optimized for cancer gene analysis.
array CGH
(39 times)
Neoplasms
(10 times)
CNVs (6 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.
array-based CGH
(5 times)
Neoplasms
(4 times)
HCC (2 times)
CGH (1 time)
EIM (1 time)
2007 High-resolution mapping of copy number aberrations and identification of target genes in hepatocellular carcinoma.
authors conducted microarray-based comparative genomic hybridization
(5 times)
Reproduction
(1 time)
FISH (2 times)
SNP (2 times)
DLRSpread (1 time)
2010 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.
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.
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.
address this question, we utilized microarray comparative genomic hybridization
(1 time)
Pathology
(1 time)
--- 2014 Comparative genomic hybridization in a case of melanoma that loses expression of S100, HMB45, Melan A and tyrosinase in metastasis.
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.
aims to describe how microarray comparative genomic hybridization
(1 time)
Gynecology
(1 time)
--- 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)
Laboratory Techniques and Procedures
(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  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.
19  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.
20  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.
21  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.
22  artificial chromosome microarray comparative genomic hybridisation
(1 time)
Laboratory Techniques and Procedures
(1 time)
--- 2007 Evaluation of Phi29-based whole-genome amplification for microarray-based comparative genomic hybridisation.
23  CGH and microarray-CGH
(1 time)
Reproductive Medicine
(1 time)
CGH (1 time)
FISH (1 time)
TE (1 time)
2011 Cytogenetic analysis of human blastocysts with the use of FISH, CGH and aCGH: scientific data and technical evaluation.
24  cytogenetics and comparative genomic hybridization
(1 time)
Neoplasms
(1 time)
EGFR (1 time)
PN (1 time)
2019 High level EGFR amplification in a newly established glioblastoma cell line 170-MG-BA.
25  HER2-amplified cancers using tiling path microarray-based comparative genomic hybridization
(1 time)
Pathology
(1 time)
--- 2008 The genomic profile of HER2-amplified breast cancers: the influence of ER status.
26  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.