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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...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2004
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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 |
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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 |
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