Evidence map›Paper›PMID 39240541›Full record

ArticleGenomics, proteomics & bioinformatics2024

TransCell: In Silico Characterization of Genomic Landscape and Cellular Responses by Deep Transfer Learning.

Shan-Ju Yeh, Shreya Paithankar, Ruoqiao Chen, Jing Xing, Mengying Sun, Ke Liu, Jiayu Zhou, Bin Chen

Abstract read
In one paragraph

Article in Genomics, proteomics & bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

8 authors.

Shan-Ju YehDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI 49503, USA.ORCID 0000-0001-7006-6396
Shreya PaithankarDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI 49503, USA.ORCID 0000-0002-9247-7847
Ruoqiao ChenDepartment of Pharmacology and Toxicology, Michigan State University, Grand Rapids, MI 49503, USA.ORCID 0000-0001-9797-1046
Jing XingDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI 49503, USA.ORCID 0000-0003-4726-8525
Mengying SunDepartment of Computer Science and Engineering, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0002-8947-0345
Ke LiuDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI 49503, USA.ORCID 0000-0003-3190-1656
Jiayu ZhouDepartment of Computer Science and Engineering, Michigan State University, East Lansing, MI 48824, USA.ORCID 0000-0003-4336-6777
Bin ChenDepartment of Pediatrics and Human Development, Michigan State University, Grand Rapids, MI 49503, USA.ORCID 0000-0001-8858-874X

Funding

Repurpose open data to discover therapeutics for understudied diseasesR01GM134307 · NIGMS · MICHIGAN STATE UNIVERSITY · PI CHEN, BIN · 2019 to 2023
$2.5M
Integrating transcriptomic, proteomic and pharmacogenomic data to inform individualized therapy in cancersK01ES028047 · NIEHS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CHEN, BIN · 2017 to 2020
$682k
NIEHS NIH HHS K01 ES028047NIGMS NIH HHS R01 GM134307
6 · The paper itself

Abstract

Gene expression profiling of new or modified cell lines becomes routine today; however, obtaining comprehensive molecular characterization and cellular responses for a variety of cell lines, including those derived from underrepresented groups, is not trivial when resources are minimal. Using gene expression to predict other measurements has been actively explored; however, systematic investigation of its predictive power in various measurements has not been well studied. Here, we evaluated commonly used machine learning methods and presented TransCell, a two-step deep transfer learning framework that utilized the knowledge derived from pan-cancer tumor samples to predict molecular features and responses. Among these models, TransCell had the best performance in predicting metabolite, gene effect score (or genetic dependency), and drug sensitivity, and had comparable performance in predicting mutation, copy number variation, and protein expression. Notably, TransCell improved the performance by over 50% in drug sensitivity prediction and achieved a correlation of 0.7 in gene effect score prediction. Furthermore, predicted drug sensitivities revealed potential repurposing candidates for new 100 pediatric cancer cell lines, and predicted gene effect scores reflected BRAF resistance in melanoma cell lines. Together, we investigated the predictive power of gene expression in six molecular measurement types and developed a web portal (http://apps.octad.org/transcell/) that enables the prediction of 352,000 genomic and cellular response features solely from gene expression profiles.

Indexed as

Deep LearningNeoplasmsCell Line, TumorComputational BiologyComputer SimulationDNA Copy Number VariationsGene Expression ProfilingGenomicsHumansCancer dependencyDrug repurposingGenomicsTranscriptomicsTransfer learning

Identifiers

PMID39240541
PMCPMC11378636

What OpenQuestion holds

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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.