Results 11 to 20 of about 91,462 (268)

Analysis of tiling array expression studies with flexible designs in Bioconductor (waveTiling) [PDF]

open access: yes, 2012
Background Existing statistical methods for tiling array transcriptome data either focus on transcript discovery in one biological or experimental condition or on the detection of differential expression between two conditions.
Thas Olivier   +6 more
core   +4 more sources

A distortion metric for the lossy compression of DNA microarray images [PDF]

open access: yes, 2013
DNA microarrays are state-of-the-art tools in biological and medical research. In this work, we discuss the suitability of lossy compression for DNA microarray images and highlight the necessity for a distortion metric to assess the loss of relevant ...
Marcellin, Michael W.   +3 more
core   +1 more source

Profiling and validation of individual and patterns of Chlamydia trachomatis-specific antibody responses in trachomatous trichiasis. [PDF]

open access: yes, 2017
BACKGROUND: Ocular Chlamydia trachomatis (Ct) infection causes trachoma, the leading infectious cause of blindness. A Ct D/UW3 proteome microarray and sera from Gambian adults with trachomatous trichiasis (TT) or healthy matched controls previously ...
Makalo, P.   +27 more
core   +1 more source

Comparison of microarray and SAGE techniques in gene expression analysis of human glioblastoma [PDF]

open access: yesCytology and Genetics, 2007
To enhance glioblastoma (GB) marker discovery we compared gene expression in GB with human normal brain (NB) by accessing SAGE Genie web site and compared obtained results with published data. Nine GB and five NB SAGE-libraries were analyzed using the Digital Gene Expression Displayer (DGED), the results of DGED were tested by Northern blot analysis ...
Kavsan, V.M.   +9 more
openaire   +4 more sources

Oncogenic pathways in hereditary and sporadic breast cancer. [PDF]

open access: yes, 2004
Cancer is a genetic disease. Breast cancer tumorigenesis can be described as a multi-step process in which each step is thought to correlate with one or more distinct mutations in major regulatory genes.
P. Kenemans   +7 more
core   +1 more source

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies

open access: yesJornal de Pediatria (Versão em Português), 2015
Objectives: Clinical use of microarray‐based techniques for the analysis of many developmental disorders has emerged during the last decade. Thus, chromosomal microarray has been positioned as a first‐tier test. This study reports the first experience in
Guillermo Lay‐Son   +5 more
doaj   +3 more sources

Automatic Spot Identification Method for High Throughput Surface Plasmon Resonance Imaging Analysis

open access: yesBiosensors, 2018
An automatic spot identification method is developed for high throughput surface plasmon resonance imaging (SPRi) analysis. As a combination of video accessing, image enhancement, image processing and parallel processing techniques, the method can ...
Zhiyou Wang   +2 more
doaj   +1 more source

EMAAS: An extensible grid-based Rich Internet Application for microarray data analysis and management

open access: yesBMC Bioinformatics, 2008
Background Microarray experimentation requires the application of complex analysis methods as well as the use of non-trivial computer technologies to manage the resultant large data sets.
Aitman T   +15 more
doaj   +1 more source

A genomic approach to identify genes associated with calcification in Emiliania huxleyi [PDF]

open access: yes, 2014
The aim of this study is to identify genes involved in calcification and coccolith production in Emiliania huxleyi using Suppressive Subtractive Hybridization (SSH) and microarray analysis techniques.
Nguyen, Binh T
core   +3 more sources

The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

open access: yesEgyptian Journal of Medical Human Genetics, 2018
Background: Rearrangements that occur mainly through the non-allelic homologous recombination (NAHR) during maternal meiosis in short arms of chromosome 8 is relatively associated with various clinical spectrum.
Fatma Silan   +6 more
doaj   +1 more source

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