Evidence map›Paper›PMID 41510020›Full record

ArticleBioinformatics advances2026

Data-based clustering in prediction of cervical cancer DNA methylation using pan-cancer genetic and clinical data.

Nidhi Pai, J Sunil Rao

Abstract read
In one paragraph

Article in Bioinformatics advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Nidhi PaiDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, MN 55414, United States.ORCID https://orcid.org/0000-0003-0187-4407
J Sunil RaoDivision of Biostatistics and Health Data Science, University of Minnesota, Minneapolis, MN 55414, United States.ORCID https://orcid.org/0000-0002-6450-3200

Funding

Biostatistics in Genetics and Genomics Training ProgramT32GM132063 · NIGMS · UNIVERSITY OF MINNESOTA · PI BASU, SAONLI, PAN, WEI · 2020 to 2024
$1.3M
NIGMS NIH HHS T32 GM132063
6 · The paper itself

Abstract

Motivation: Understanding the role of DNA methylation in oncogenesis, diagnosis, and treatment requires data sufficient in size and accuracy, but current epigenetic data is limited, especially for population groups underrepresented in research. We propose a framework for generating highly accurate DNA methylation predictions using classified mixed model prediction, incorporating a step to cluster patients into cross-cancer and cross-race groups. Results: Simulations show our framework more accurately predicts underlying mixed effects compared to regression prediction and naive estimates, extending previous work to the case where clusters are estimated from the data. We illustrate this framework using data from The Cancer Genome Atlas, uncovering clustering patterns and generating DNA methylation predictions for further analysis. Our work demonstrates how shared random effects can be leveraged to borrow strength across observations with similar methylation patterns. Availability and implementation: The methods are implemented in R and available at: https://github.com/nidhipai/dnam_cmmp.

Identifiers

PMID41510020
PMCPMC12776347

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.