Evidence map›Paper›PMID 40967222›Full record

ArticleAmerican journal of human genetics2025

Unveiling tissue heterogeneity through genomic interaction-encoded image representation of RNA-sequencing data.

Junyan Liu, Zixia Zhou, Yizheng Chen, Md Tauhidul Islam, Lei Xing

Abstract read
In one paragraph

Article in American journal of human genetics, 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. 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

5 authors.

Junyan LiuDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, USA.
Zixia ZhouDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, USA.
Yizheng ChenDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, USA.
Md Tauhidul IslamDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, USA. Electronic address: tauhid@stanford.edu.
Lei XingDepartment of Radiation Oncology, Stanford University, Stanford, CA 94305, USA. Electronic address: lei@stanford.edu.

Funding

Radioluminescence dosimetry solution for precision radiation therapyR01CA223667 · NCI · STANFORD UNIVERSITY · PI XING, LEI · 2018 to 2022
$2.4M
DASSIM-RT and Compressed Sensing-Based Inverse PlanningR01CA176553 · NCI · STANFORD UNIVERSITY · PI XING, LEI · 2014 to 2018
$2.4M
Development of AI-Augmented quality assurance tools for radiation therapyR01CA275772 · NCI · STANFORD UNIVERSITY · PI Lei Xing · 2023 to 2026
$2.1M
High-performance deep neural networks for medical image analysisK99LM014309 · NLM · STANFORD UNIVERSITY · PI ISLAM, MD TAUHIDUL · 2023 to 2024
$178k
NCI NIH HHS R01 CA176553NCI NIH HHS R01 CA223667NCI NIH HHS R01 CA275772NLM NIH HHS K99 LM014309
6 · The paper itself

Abstract

Genomic sequencing is essential for both biomedical research and clinical practice. While single-cell RNA sequencing (scRNA-seq) provides insights into biological processes at the cellular level, bulk RNA sequencing remains widely used for its scalability and cost-effectiveness. To explore biological heterogeneity, research efforts have been made toward inferring single-cell-like cellular compositions from bulk samples, i.e., deconvolving bulk samples into multiple cell types. However, existing deconvolution methods face two major limitations: (1) reliance on predefined gene signature matrices without accounting for inter-sample variability and (2) susceptibility to noise within biological systems. Here, we propose a cellular-component analysis (CCA) framework by leveraging a genomic-interaction-encoded image representation of RNA-seq data for substantially improved pattern discovery. The framework incorporates sample-specific gene-expression variability and derives signature patterns by utilizing a convolutional variational autoencoder and Gaussian mixture model. An image-domain linear decomposition of bulk RNA-seq data based on these sample-specific, interpretable gene-signature patterns is then performed for CCA and other downstream tasks, such as cancer subtype classification and biomarker discovery. We demonstrate that the proposed technique improves decomposition accuracy by over 14.1% in average Pearson correlation compared to existing techniques by using both simulation and experimental datasets. This approach offers an effective solution for tissue heterogeneity analysis and lays a foundation for a range of clinical and biological applications.

Indexed as

GenomicsSequence Analysis, RNASingle-Cell AnalysisAlgorithmsGene Expression ProfilingHumansNeoplasmsdecompositiondeep learningRNA sequencing

Identifiers

PMID40967222
PMCPMC12609178

What OpenQuestion holds

Textmetadata
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.