Evidence map›Paper›PMID 40465796›Full record

ArticlePLoS computational biology2025

DeepDeconUQ estimates malignant cell fraction prediction intervals in bulk RNA-seq tissue.

Jiawei Huang, Yuxuan Du, Kevin R Kelly, Jinchi Lv, Yingying Fan, Jiang F Zhong, Fengzhu Sun

Abstract read
In one paragraph

Article in PLoS computational biology, 2025. 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. Review
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.

Jiawei HuangDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, California, United States of America.
Yuxuan DuDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, California, United States of America.
Kevin R KellyDivision of Hematology, University of Southern California, Los Angeles, California, United States of America.
Jinchi LvData Sciences and Operations Department, University of Southern California, Los Angeles, California, United States of America.
Yingying FanData Sciences and Operations Department, University of Southern California, Los Angeles, California, United States of America.
Jiang F ZhongDepartment of Basic Sciences, School of Medicine, Loma Linda University, Loma Linda, California, United States of America.
Fengzhu SunDepartment of Quantitative and Computational Biology, University of Southern California, Los Angeles, California, United States of America.ORCID 0000-0002-8552-043X

Funding

Supplement: Large scale single-cell gene rearrangement detection with a microfluidic deviceR01CA251848 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHONG, JOHN · 2020 to 2025
$2.4M
Molecular Characteristics of Treatment-resistant High-risk NeuroblastomaR01CA197903 · NCI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI ZHONG, JOHN · 2016 to 2020
$1.9M
NCI NIH HHS R01 CA197903NCI NIH HHS R01 CA251848
6 · The paper itself

Abstract

Accurate estimation of malignant cell fractions in tissues plays a critical role in cancer diagnosis, prognosis, and subsequent treatment decisions. However, most currently available methods provide only point estimates, neglecting the quantification of uncertainties, which is essential for both clinical and research applications. This study introduces DeepDeconUQ, a deep neural network model developed to estimate prediction intervals for malignant cell fractions based on bulk RNA-seq data. This approach addresses limitations in current malignant cell fraction estimation methods by integrating uncertainty quantification into predictions of cancer cell fractions. DeepDeconUQ leverages single-cell RNA sequencing (scRNA-seq) data in conjunction with conformalized quantile regression to produce reliable prediction intervals. The model trains a quantile regression neural network to establish upper and lower bounds for cancer cell proportions, followed by a calibration step that refines these intervals to ensure both statistical validity (coverage probability) and discrimination (narrow intervals). Benchmark analyses indicate that DeepDeconUQ consistently surpasses existing methods, achieving high coverage accuracy with tight prediction intervals across simulated and real cancer datasets. The robustness of DeepDeconUQ is further demonstrated by its resilience to various gene expression perturbations. The DeepDeconUQ method is publicly accessible at https://github.com/jiaweih14/DeepDeconUQ.

Indexed as

NeoplasmsRNA-SeqSequence Analysis, RNAComputational BiologyDeep LearningHumansNeural Networks, ComputerSingle-Cell Analysis

Identifiers

PMID40465796
PMCPMC12162100

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.