Evidence map›Paper›PMID 36259664›Full record

ArticleNucleic acids research2023

CREAMMIST: an integrative probabilistic database for cancer drug response prediction.

Hatairat Yingtaweesittikul, Jiaxi Wu, Aanchal Mongia, Rafael Peres, Karrie Ko, Niranjan Nagarajan, Chayaporn Suphavilai

Abstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

  1. Harmonization and integration of pharmacogenomics screens.Bioinformatics (Oxford, England) · 2026
    Article
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  7. Review
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  9. Cancer pharmacoinformatics: Databases and analytical tools.Functional & integrative genomics · 2024
    Review
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  11. Article
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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.

Hatairat YingtaweesittikulAdvanced Research Center for Computational Simulation, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand.
Jiaxi WuGenome Institute of Singapore, A*STAR, Singapore, Singapore.
Aanchal MongiaGenome Institute of Singapore, A*STAR, Singapore, Singapore.
Rafael PeresGenome Institute of Singapore, A*STAR, Singapore, Singapore.
Karrie KoGenome Institute of Singapore, A*STAR, Singapore, Singapore.
Niranjan NagarajanGenome Institute of Singapore, A*STAR, Singapore, Singapore.
Chayaporn SuphavilaiGenome Institute of Singapore, A*STAR, Singapore, Singapore.ORCID 0000-0002-4777-4586

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extensive in vitro cancer drug screening datasets have enabled scientists to identify biomarkers and develop machine learning models for predicting drug sensitivity. While most advancements have focused on omics profiles, cancer drug sensitivity scores precalculated by the original sources are often used as-is, without consideration for variabilities between studies. It is well-known that significant inconsistencies exist between the drug sensitivity scores across datasets due to differences in experimental setups and preprocessing methods used to obtain the sensitivity scores. As a result, many studies opt to focus only on a single dataset, leading to underutilization of available data and a limited interpretation of cancer pharmacogenomics analysis. To overcome these caveats, we have developed CREAMMIST (https://creammist.mtms.dev), an integrative database that enables users to obtain an integrative dose-response curve, to capture uncertainty (or high certainty when multiple datasets well align) across five widely used cancer cell-line drug-response datasets. We utilized the Bayesian framework to systematically integrate all available dose-response values across datasets (>14 millions dose-response data points). CREAMMIST provides easy-to-use statistics derived from the integrative dose-response curves for various downstream analyses such as identifying biomarkers, selecting drug concentrations for experiments, and training robust machine learning models.

Indexed as

Antineoplastic AgentsDatabases, FactualNeoplasmsBayes TheoremBiomarkersHumansMachine LearningAntineoplastic AgentsBiomarkers

Identifiers

PMID36259664
PMCPMC9825458

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Registered trials

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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.