Evidence map›Paper›PMID 29949984›Full record

ArticleBioinformatics (Oxford, England)2018

Improving genomics-based predictions for precision medicine through active elicitation of expert knowledge.

Iiris Sundin, Tomi Peltola, Luana Micallef, Homayun Afrabandpey, Marta Soare, Muntasir Mamun Majumder, Pedram Daee, Chen He, Baris Serim, Aki Havulinna and 4 more

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

14 authors.

Iiris SundinDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Tomi PeltolaDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Luana MicallefDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Homayun AfrabandpeyDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Marta SoareDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Muntasir Mamun MajumderInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Pedram DaeeDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Chen HeDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, University of Helsinki, Helsinki, Finland.
Baris SerimDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, University of Helsinki, Helsinki, Finland.
Aki HavulinnaInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Caroline HeckmanInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Giulio JacucciDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, University of Helsinki, Helsinki, Finland.
Pekka MarttinenDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.
Samuel KaskiDepartment of Computer Science, Helsinki Institute for Information Technology HIIT, Aalto University, Helsinki, Finland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Precision medicine requires the ability to predict the efficacies of different treatments for a given individual using high-dimensional genomic measurements. However, identifying predictive features remains a challenge when the sample size is small. Incorporating expert knowledge offers a promising approach to improve predictions, but collecting such knowledge is laborious if the number of candidate features is very large. Results: We introduce a probabilistic framework to incorporate expert feedback about the impact of genomic measurements on the outcome of interest and present a novel approach to collect the feedback efficiently, based on Bayesian experimental design. The new approach outperformed other recent alternatives in two medical applications: prediction of metabolic traits and prediction of sensitivity of cancer cells to different drugs, both using genomic features as predictors. Furthermore, the intelligent approach to collect feedback reduced the workload of the expert to approximately 11%, compared to a baseline approach. Availability and implementation: Source code implementing the introduced computational methods is freely available at https://github.com/AaltoPML/knowledge-elicitation-for-precision-medicine. Supplementary information: Supplementary data are available at Bioinformatics online.

Indexed as

SoftwareBayes TheoremGenomicsHumansPrecision MedicineSequence Analysis, DNA

Identifiers

PMID29949984
PMCPMC6022689

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.