Evidence map›Paper›PMID 19542156›Full record

ArticleBioinformatics (Oxford, England)2009

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

Gerald Quon, Quaid Morris

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

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  16. Personalized medicine: from genotypes and molecular phenotypes towards therapy- session introduction.Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing · 2014
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Gerald QuonDepartment of Computer Science, University of Toronto, Toronto, Canada. gerald.quon@utoronto.ca
Quaid Morris

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationOne 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.

resultsWe 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.

Indexed as

SoftwareComputational BiologyGene Expression ProfilingNeoplasmsOligonucleotide Array Sequence Analysis

Identifiers

PMID19542156
PMCPMC2781747

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.