Evidence map›Paper›PMID 25972088›Full record

ArticleBMC bioinformatics2015

ISOpureR: an R implementation of a computational purification algorithm of mixed tumour profiles.

Catalina V Anghel, Gerald Quon, Syed Haider, Francis Nguyen, Amit G Deshwar, Quaid D Morris, Paul C Boutros

Abstract read
In one paragraph

Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed.

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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

7 authors.

Catalina V AnghelInformatics and Biocomputing Program, Ontario Institute for Cancer Research, 661 University Avenue, Toronto, Suite 510, M5G 0A3, ON, Canada. Catalina.Anghel@oicr.on.ca.
Gerald QuonDepartment of Computer Science, University of Toronto, 10 King's College Road, Room 3303, M5S 3G4, Toronto, ON, Canada. gquon@mit.edu.
Syed HaiderInformatics and Biocomputing Program, Ontario Institute for Cancer Research, 661 University Avenue, Toronto, Suite 510, M5G 0A3, ON, Canada. Syed.Haider@oicr.on.ca.
Francis NguyenInformatics and Biocomputing Program, Ontario Institute for Cancer Research, 661 University Avenue, Toronto, Suite 510, M5G 0A3, ON, Canada. F-Nguyen@hotmail.com.
Amit G DeshwarEdward S. Rogers Sr. Department of Electrical and Computer Engineering, University of Toronto, 10 King's College, Room SFB540, Toronto, M5S 3G4, ON, Canada. Amit.Deshwar@utoronto.ca.
Quaid D MorrisDepartment of Computer Science, University of Toronto, 10 King's College Road, Room 3303, M5S 3G4, Toronto, ON, Canada. Quaid.Morris@utoronto.ca.
Paul C BoutrosInformatics and Biocomputing Program, Ontario Institute for Cancer Research, 661 University Avenue, Toronto, Suite 510, M5G 0A3, ON, Canada. Paul.Boutros@oicr.on.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumour samples containing distinct sub-populations of cancer and normal cells present challenges in the development of reproducible biomarkers, as these biomarkers are based on bulk signals from mixed tumour profiles. ISOpure is the only mRNA computational purification method to date that does not require a paired tumour-normal sample, provides a personalized cancer profile for each patient, and has been tested on clinical data. Replacing mixed tumour profiles with ISOpure-preprocessed cancer profiles led to better prognostic gene signatures for lung and prostate cancer.

resultsTo simplify the integration of ISOpure into standard R-based bioinformatics analysis pipelines, the algorithm has been implemented as an R package. The ISOpureR package performs analogously to the original code in estimating the fraction of cancer cells and the patient cancer mRNA abundance profile from tumour samples in four cancer datasets.

conclusionsThe ISOpureR package estimates the fraction of cancer cells and personalized patient cancer mRNA abundance profile from a mixed tumour profile. This open-source R implementation enables integration into existing computational pipelines, as well as easy testing, modification and extension of the model.

Indexed as

AlgorithmsGene Expression ProfilingSoftwareComputational BiologyHumansMaleModels, TheoreticalPrognosisProstatic Neoplasms

Identifiers

PMID25972088
PMCPMC4429941

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LicenceCC BY
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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.