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Article: Analysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis

TitleAnalysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis
Authors
KeywordsAfrican Americans
breast cancer
discriminant analysis
health disparities
microarrays
oestrogen receptor
Issue Date2010
Citation
Human Genomics, 2010, v. 5 n. 1, p. 5-16 How to Cite?
AbstractBreast cancer tumours among African Americans are usually more aggressive than those found in Caucasian populations. African-American patients with breast cancer also have higher mortality rates than Caucasian women. A better understanding of the disease aetiology of these breast cancers can help to improve and develop new methods for cancer prevention, diagnosis and treatment. The main goal of this project was to identify genes that help differentiate between oestrogen receptor-positive and -negative samples among a small group of African-American patients with breast cancer. Breast cancer microarrays from one of the largest genomic consortiums were analysed using 13 African-American and 201 Caucasian samples with oestrogen receptor status. We used a shrinkage-based classification method to identify genes that were informative in discriminating between oestrogen receptor-positive and -negative samples. Subset analysis and permutation were performed to obtain a set of genes unique to the African-American population. We identified a set of 156 probe sets, which gave a misclassification rate of 0.16 in distinguishing between oestrogen receptor-positive and -negative patients. The biological relevance of our findings was explored through literature-mining techniques and pathway mapping. An independent dataset was used to validate our findings and we found that the top ten genes mapped onto this dataset gave a misclassification rate of 0.15. The described method allows us best to utilise the information available from small sample size microarray data in the context of ethnic minorities.
Persistent Identifierhttp://hdl.handle.net/10722/194509
ISSN
2021 Impact Factor: 6.481
2020 SCImago Journal Rankings: 1.414

 

DC FieldValueLanguage
dc.contributor.authorPang, H-
dc.contributor.authorEbisu, K-
dc.contributor.authorWatanabe, E-
dc.contributor.authorSue, LY-
dc.contributor.authorTong, T-
dc.date.accessioned2014-01-30T03:32:40Z-
dc.date.available2014-01-30T03:32:40Z-
dc.date.issued2010-
dc.identifier.citationHuman Genomics, 2010, v. 5 n. 1, p. 5-16-
dc.identifier.issn1473-9542-
dc.identifier.urihttp://hdl.handle.net/10722/194509-
dc.description.abstractBreast cancer tumours among African Americans are usually more aggressive than those found in Caucasian populations. African-American patients with breast cancer also have higher mortality rates than Caucasian women. A better understanding of the disease aetiology of these breast cancers can help to improve and develop new methods for cancer prevention, diagnosis and treatment. The main goal of this project was to identify genes that help differentiate between oestrogen receptor-positive and -negative samples among a small group of African-American patients with breast cancer. Breast cancer microarrays from one of the largest genomic consortiums were analysed using 13 African-American and 201 Caucasian samples with oestrogen receptor status. We used a shrinkage-based classification method to identify genes that were informative in discriminating between oestrogen receptor-positive and -negative samples. Subset analysis and permutation were performed to obtain a set of genes unique to the African-American population. We identified a set of 156 probe sets, which gave a misclassification rate of 0.16 in distinguishing between oestrogen receptor-positive and -negative patients. The biological relevance of our findings was explored through literature-mining techniques and pathway mapping. An independent dataset was used to validate our findings and we found that the top ten genes mapped onto this dataset gave a misclassification rate of 0.15. The described method allows us best to utilise the information available from small sample size microarray data in the context of ethnic minorities.-
dc.languageeng-
dc.relation.ispartofHuman Genomics-
dc.subjectAfrican Americans-
dc.subjectbreast cancer-
dc.subjectdiscriminant analysis-
dc.subjecthealth disparities-
dc.subjectmicroarrays-
dc.subjectoestrogen receptor-
dc.titleAnalysing breast cancer microarrays from African Americans using shrinkage-based discriminant analysis-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1186/1479-7364-5-1-5-
dc.identifier.pmid21106486-
dc.identifier.scopuseid_2-s2.0-79952278307-
dc.identifier.volume5-
dc.identifier.issue1-
dc.identifier.spage5-
dc.identifier.epage16-
dc.identifier.issnl1473-9542-

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