Results 21 to 30 of about 88,145 (306)

Image analysis in comparative genomic hybridization [PDF]

open access: yesCytometry, 1995
AbstractComparative genomic hybridization (CGH) is a new technique by which genomic imbalances can be detected by combining in situ suppression hybridization of whole genomic DNA and image analysis. We have developed software for rapid, quantitative CGH image analysis by a modification and extension of the standard software used for routine karyotyping
C, Lundsteen   +6 more
openaire   +2 more sources

Comparative genomics in chicken and Pekin duck using FISH mapping and microarray analysis [PDF]

open access: yes, 2009
BACKGROUND: The availability of the complete chicken (Gallus gallus) genome sequence as well as a large number of chicken probes for fluorescent in-situ hybridization (FISH) and microarray resources facilitate comparative genomic studies between ...
Ioannou, D.   +30 more
core   +1 more source

A novel deletion in 2q24.1q24.2 in a girl with mental retardation and generalized hypotonia: a case report

open access: yesMolecular Cytogenetics, 2012
Background Chromosomal imbalances, recognized as the major cause of mental retardation, are often due to submicroscopic deletions or duplications not evidenced by conventional cytogenetic methods.
Palumbo Orazio   +5 more
doaj   +1 more source

Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience

open access: yesCancer Medicine, 2018
A genomic index (GI) tool using array comparative genomic hybridization (aCGH) on tumor cells has emerged as independent prognostic factor associated with the risk of metastatic relapse in synovial sarcoma (SS).
Daniel Orbach   +13 more
doaj   +1 more source

Prenatal diagnosis and molecular cytogenetic characterization of three chromosomal abnormalities with favorable outcomes

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2020
Objective: Here we present three cases of chromosomal abnormalities with favorable outcomes. Case report: In Case 1, conventional karyotyping revealed a karyotype of 46, XY,t(7; 14) (q35; q13)[4]/46,XY[26].
Qiuqing Chen   +4 more
doaj   +1 more source

The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary [PDF]

open access: yes, 1994
Fluorescencein situ hybridization (FISH) of microlibraries established from distinct chromosome subregions can test the evolutionary conservation of chromosome bands as well as chromosomal rearrangements that occurred during primate evolution and will ...
Cremer, Thomas   +8 more
core   +1 more source

Comparative genomic hybridization of postirradiation sarcomas [PDF]

open access: yesCancer, 2001
Radiotherapy is a known risk factor for sarcoma development. Postirradiation sarcomas arise within the radiation field after a latency period of several years and usually are highly malignant. Very little is yet known about their genetic changes.Twenty-seven postirradiation sarcomas were analyzed by comparative genomic hybridization, which allows ...
M, Tarkkanen   +10 more
openaire   +2 more sources

Chromosomal imbalances detected in primary bone tumors by comparative genomic hybridization and interphase fluorescence in situ hybridization

open access: yesGenetics and Molecular Biology, 2003
We applied a combination of comparative genomic hybridization (CGH) and fluorescence in situ hybridization (FISH), to characterize the genetic aberrations in three osteosarcomas (OS) and one Ewing's sarcoma. CGH identified recurrent chromosomal losses at
Marcelo Razera Baruffi   +4 more
doaj   +1 more source

CGHpower: exploring sample size calculations for chromosomal copy number experiments [PDF]

open access: yes, 2010
Background Determining a suitable sample size is an important step in the planning of microarray experiments. Increasing the number of arrays gives more statistical power, but adds to the total cost of the experiment.
Scheinin, A.I.   +24 more
core   +1 more source

High Resolution Comparative Genomic Hybridization Detects 7–8 Megabasepair Deletion in PCR Amplified DNA1

open access: yesAnalytical Cellular Pathology, 2001
We investigated if any change in spatial resolution of comparative genomic hybridization analysis could be detected when using DNA amplified by degenerate oligonucleotide primed PCR (DOP‐PCR) as opposed to the use of unamplified DNA.
Jacob Larsen   +4 more
doaj   +1 more source

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