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Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays
BACKGROUND: Genome-wide detection of single feature polymorphisms (SFP) in swine using transcriptome profiling of day 25 placental RNA by contrasting probe intensities from either Meishan or an occidental composite breed with Affymetrix porcine microarrays is presented. A linear mixed model analysis...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442091/ https://www.ncbi.nlm.nih.gov/pubmed/18510738 http://dx.doi.org/10.1186/1471-2164-9-252 |
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author | Bischoff, Steve R Tsai, Shengdar Hardison, Nicholas E York, Abby M Freking, Brad A Nonneman, Dan Rohrer, Gary Piedrahita, Jorge A |
author_facet | Bischoff, Steve R Tsai, Shengdar Hardison, Nicholas E York, Abby M Freking, Brad A Nonneman, Dan Rohrer, Gary Piedrahita, Jorge A |
author_sort | Bischoff, Steve R |
collection | PubMed |
description | BACKGROUND: Genome-wide detection of single feature polymorphisms (SFP) in swine using transcriptome profiling of day 25 placental RNA by contrasting probe intensities from either Meishan or an occidental composite breed with Affymetrix porcine microarrays is presented. A linear mixed model analysis was used to identify significant breed-by-probe interactions. RESULTS: Gene specific linear mixed models were fit to each of the log(2 )transformed probe intensities on these arrays, using fixed effects for breed, probe, breed-by-probe interaction, and a random effect for array. After surveying the day 25 placental transcriptome, 857 probes with a q-value ≤ 0.05 and |fold change| ≥ 2 for the breed-by-probe interaction were identified as candidates containing SFP. To address the quality of the bioinformatics approach, universal pyrosequencing assays were designed from Affymetrix exemplar sequences to independently assess polymorphisms within a subset of probes for validation. Additionally probes were randomly selected for sequencing to determine an unbiased confirmation rate. In most cases, the 25-mer probe sequence printed on the microarray diverged from Meishan, not occidental crosses. This analysis was used to define a set of highly reliable predicted SFPs according to their probability scores. CONCLUSION: By applying a SFP detection method to two mammalian breeds for the first time, we detected transition and transversion single nucleotide polymorphisms, as well as insertions/deletions which can be used to rapidly develop markers for genetic mapping and association analysis in species where high density genotyping platforms are otherwise unavailable. SNPs and INDELS discovered by this approach have been publicly deposited in NCBI's SNP repository dbSNP. This method is an attractive bioinformatics tool for uncovering breed-by-probe interactions, for rapidly identifying expressed SNPs, for investigating potential functional correlations between gene expression and breed polymorphisms, and is robust enough to be used on any Affymetrix gene expression platform. |
format | Text |
id | pubmed-2442091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24420912008-07-01 Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays Bischoff, Steve R Tsai, Shengdar Hardison, Nicholas E York, Abby M Freking, Brad A Nonneman, Dan Rohrer, Gary Piedrahita, Jorge A BMC Genomics Methodology Article BACKGROUND: Genome-wide detection of single feature polymorphisms (SFP) in swine using transcriptome profiling of day 25 placental RNA by contrasting probe intensities from either Meishan or an occidental composite breed with Affymetrix porcine microarrays is presented. A linear mixed model analysis was used to identify significant breed-by-probe interactions. RESULTS: Gene specific linear mixed models were fit to each of the log(2 )transformed probe intensities on these arrays, using fixed effects for breed, probe, breed-by-probe interaction, and a random effect for array. After surveying the day 25 placental transcriptome, 857 probes with a q-value ≤ 0.05 and |fold change| ≥ 2 for the breed-by-probe interaction were identified as candidates containing SFP. To address the quality of the bioinformatics approach, universal pyrosequencing assays were designed from Affymetrix exemplar sequences to independently assess polymorphisms within a subset of probes for validation. Additionally probes were randomly selected for sequencing to determine an unbiased confirmation rate. In most cases, the 25-mer probe sequence printed on the microarray diverged from Meishan, not occidental crosses. This analysis was used to define a set of highly reliable predicted SFPs according to their probability scores. CONCLUSION: By applying a SFP detection method to two mammalian breeds for the first time, we detected transition and transversion single nucleotide polymorphisms, as well as insertions/deletions which can be used to rapidly develop markers for genetic mapping and association analysis in species where high density genotyping platforms are otherwise unavailable. SNPs and INDELS discovered by this approach have been publicly deposited in NCBI's SNP repository dbSNP. This method is an attractive bioinformatics tool for uncovering breed-by-probe interactions, for rapidly identifying expressed SNPs, for investigating potential functional correlations between gene expression and breed polymorphisms, and is robust enough to be used on any Affymetrix gene expression platform. BioMed Central 2008-05-29 /pmc/articles/PMC2442091/ /pubmed/18510738 http://dx.doi.org/10.1186/1471-2164-9-252 Text en Copyright © 2008 Bischoff et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Bischoff, Steve R Tsai, Shengdar Hardison, Nicholas E York, Abby M Freking, Brad A Nonneman, Dan Rohrer, Gary Piedrahita, Jorge A Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays |
title | Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays |
title_full | Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays |
title_fullStr | Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays |
title_full_unstemmed | Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays |
title_short | Identification of SNPs and INDELS in swine transcribed sequences using short oligonucleotide microarrays |
title_sort | identification of snps and indels in swine transcribed sequences using short oligonucleotide microarrays |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442091/ https://www.ncbi.nlm.nih.gov/pubmed/18510738 http://dx.doi.org/10.1186/1471-2164-9-252 |
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