Cargando…

Improving signal intensities for genes with low-expression on oligonucleotide microarrays

BACKGROUND: DNA microarrays using long oligonucleotide probes are widely used to evaluate gene expression in biological samples. These oligonucleotides are pre-synthesized and sequence-optimized to represent specific genes with minimal cross-hybridization to homologous genes. Probe length and concen...

Descripción completa

Detalles Bibliográficos
Autores principales: Ramdas, Latha, Cogdell, David E, Jia, Jack Y, Taylor, Ellen E, Dunmire, Valerie R, Hu, Limei, Hamilton, Stanley R, Zhang, Wei
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC436055/
https://www.ncbi.nlm.nih.gov/pubmed/15196312
http://dx.doi.org/10.1186/1471-2164-5-35
_version_ 1782121528208392192
author Ramdas, Latha
Cogdell, David E
Jia, Jack Y
Taylor, Ellen E
Dunmire, Valerie R
Hu, Limei
Hamilton, Stanley R
Zhang, Wei
author_facet Ramdas, Latha
Cogdell, David E
Jia, Jack Y
Taylor, Ellen E
Dunmire, Valerie R
Hu, Limei
Hamilton, Stanley R
Zhang, Wei
author_sort Ramdas, Latha
collection PubMed
description BACKGROUND: DNA microarrays using long oligonucleotide probes are widely used to evaluate gene expression in biological samples. These oligonucleotides are pre-synthesized and sequence-optimized to represent specific genes with minimal cross-hybridization to homologous genes. Probe length and concentration are critical factors for signal sensitivity, particularly when genes with various expression levels are being tested. We evaluated the effects of oligonucleotide probe length and concentration on signal intensity measurements of the expression levels of genes in a target sample. RESULTS: Selected genes of various expression levels in a single cell line were hybridized to oligonucleotide arrays of four lengths and four concentrations of probes to determine how these critical parameters affected the intensity of the signal representing their expression. We found that oligonucleotides of longer length significantly increased the signals of genes with low-expression in the target. High-expressing gene signals were also boosted but to a lesser degree. Increasing the probe concentration, however, did not linearly increase the signal intensity for either low- or high-expressing genes. CONCLUSIONS: We conclude that the longer the oligonuclotide probe the better the signal intensities of low expressing genes on oligonucleotide arrays.
format Text
id pubmed-436055
institution National Center for Biotechnology Information
language English
publishDate 2004
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-4360552004-06-26 Improving signal intensities for genes with low-expression on oligonucleotide microarrays Ramdas, Latha Cogdell, David E Jia, Jack Y Taylor, Ellen E Dunmire, Valerie R Hu, Limei Hamilton, Stanley R Zhang, Wei BMC Genomics Research Article BACKGROUND: DNA microarrays using long oligonucleotide probes are widely used to evaluate gene expression in biological samples. These oligonucleotides are pre-synthesized and sequence-optimized to represent specific genes with minimal cross-hybridization to homologous genes. Probe length and concentration are critical factors for signal sensitivity, particularly when genes with various expression levels are being tested. We evaluated the effects of oligonucleotide probe length and concentration on signal intensity measurements of the expression levels of genes in a target sample. RESULTS: Selected genes of various expression levels in a single cell line were hybridized to oligonucleotide arrays of four lengths and four concentrations of probes to determine how these critical parameters affected the intensity of the signal representing their expression. We found that oligonucleotides of longer length significantly increased the signals of genes with low-expression in the target. High-expressing gene signals were also boosted but to a lesser degree. Increasing the probe concentration, however, did not linearly increase the signal intensity for either low- or high-expressing genes. CONCLUSIONS: We conclude that the longer the oligonuclotide probe the better the signal intensities of low expressing genes on oligonucleotide arrays. BioMed Central 2004-06-14 /pmc/articles/PMC436055/ /pubmed/15196312 http://dx.doi.org/10.1186/1471-2164-5-35 Text en Copyright © 2004 Ramdas et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Ramdas, Latha
Cogdell, David E
Jia, Jack Y
Taylor, Ellen E
Dunmire, Valerie R
Hu, Limei
Hamilton, Stanley R
Zhang, Wei
Improving signal intensities for genes with low-expression on oligonucleotide microarrays
title Improving signal intensities for genes with low-expression on oligonucleotide microarrays
title_full Improving signal intensities for genes with low-expression on oligonucleotide microarrays
title_fullStr Improving signal intensities for genes with low-expression on oligonucleotide microarrays
title_full_unstemmed Improving signal intensities for genes with low-expression on oligonucleotide microarrays
title_short Improving signal intensities for genes with low-expression on oligonucleotide microarrays
title_sort improving signal intensities for genes with low-expression on oligonucleotide microarrays
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC436055/
https://www.ncbi.nlm.nih.gov/pubmed/15196312
http://dx.doi.org/10.1186/1471-2164-5-35
work_keys_str_mv AT ramdaslatha improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT cogdelldavide improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT jiajacky improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT taylorellene improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT dunmirevalerier improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT hulimei improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT hamiltonstanleyr improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays
AT zhangwei improvingsignalintensitiesforgeneswithlowexpressiononoligonucleotidemicroarrays