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ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing

Motivation: One of the most deadly cancer diagnoses is the carcinoma of unknown primary origin. Without the knowledge of the site of origin, treatment regimens are limited in their specificity and result in high mortality rates. Though supervised classification methods have been developed to predict...

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Detalles Bibliográficos
Autores principales: Quon, Gerald, Morris, Quaid
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781747/
https://www.ncbi.nlm.nih.gov/pubmed/19542156
http://dx.doi.org/10.1093/bioinformatics/btp378
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author Quon, Gerald
Morris, Quaid
author_facet Quon, Gerald
Morris, Quaid
author_sort Quon, Gerald
collection PubMed
description Motivation: One of the most deadly cancer diagnoses is the carcinoma of unknown primary origin. Without the knowledge of the site of origin, treatment regimens are limited in their specificity and result in high mortality rates. Though supervised classification methods have been developed to predict the site of origin based on gene expression data, they require large numbers of previously classified tumors for training, in part because they do not account for sample heterogeneity, which limits their application to well-studied cancers. Results: We present ISOLATE, a new statistical method that simultaneously predicts the primary site of origin of cancers and addresses sample heterogeneity, while taking advantage of new high-throughput sequencing technology that promises to bring higher accuracy and reproducibility to gene expression profiling experiments. ISOLATE makes predictions de novo, without having seen any training expression profiles of cancers with identified origin. Compared with previous methods, ISOLATE is able to predict the primary site of origin, de-convolve and remove the effect of sample heterogeneity and identify differentially expressed genes with higher accuracy, across both synthetic and clinical datasets. Methods such as ISOLATE are invaluable tools for clinicians faced with carcinomas of unknown primary origin. Availability: ISOLATE is available for download at: http://morrislab.med.utoronto.ca/software Contact: gerald.quon@utoronto.ca; quaid.morris@utoronto.ca Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-27817472009-11-25 ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing Quon, Gerald Morris, Quaid Bioinformatics Ismb/Eccb 2009 Special Interest Group on Short Read Sequencing Motivation: One of the most deadly cancer diagnoses is the carcinoma of unknown primary origin. Without the knowledge of the site of origin, treatment regimens are limited in their specificity and result in high mortality rates. Though supervised classification methods have been developed to predict the site of origin based on gene expression data, they require large numbers of previously classified tumors for training, in part because they do not account for sample heterogeneity, which limits their application to well-studied cancers. Results: We present ISOLATE, a new statistical method that simultaneously predicts the primary site of origin of cancers and addresses sample heterogeneity, while taking advantage of new high-throughput sequencing technology that promises to bring higher accuracy and reproducibility to gene expression profiling experiments. ISOLATE makes predictions de novo, without having seen any training expression profiles of cancers with identified origin. Compared with previous methods, ISOLATE is able to predict the primary site of origin, de-convolve and remove the effect of sample heterogeneity and identify differentially expressed genes with higher accuracy, across both synthetic and clinical datasets. Methods such as ISOLATE are invaluable tools for clinicians faced with carcinomas of unknown primary origin. Availability: ISOLATE is available for download at: http://morrislab.med.utoronto.ca/software Contact: gerald.quon@utoronto.ca; quaid.morris@utoronto.ca Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2009-11-01 2009-06-19 /pmc/articles/PMC2781747/ /pubmed/19542156 http://dx.doi.org/10.1093/bioinformatics/btp378 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Ismb/Eccb 2009 Special Interest Group on Short Read Sequencing
Quon, Gerald
Morris, Quaid
ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
title ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
title_full ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
title_fullStr ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
title_full_unstemmed ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
title_short ISOLATE: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
title_sort isolate: a computational strategy for identifying the primary origin of cancers using high-throughput sequencing
topic Ismb/Eccb 2009 Special Interest Group on Short Read Sequencing
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781747/
https://www.ncbi.nlm.nih.gov/pubmed/19542156
http://dx.doi.org/10.1093/bioinformatics/btp378
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