Evidence map›Paper›PMID 39026798›Full record

ArticlebioRxiv : the preprint server for biology2024

Multi-dataset Integration and Residual Connections Improve Proteome Prediction from Transcriptomes using Deep Learning.

Caleb W Cranney, Jesse G Meyer

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. 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.

Caleb W CranneyDepartment of Computational Biomedicine, Cedars Sinai Medical Center, Los Angeles CA 90048.ORCID 0000-0001-8482-758X
Jesse G MeyerDepartment of Computational Biomedicine, Cedars Sinai Medical Center, Los Angeles CA 90048.ORCID 0000-0003-2753-3926

Funding

Democratizing Multi-Omics to Expedite Discovery of Hidden Metabolic PathwaysR35GM142502 · NIGMS · MEDICAL COLLEGE OF WISCONSIN · PI MEYER, JESSE · 2021 to 2025
$2.2M
NIGMS NIH HHS R35 GM142502
6 · The paper itself

Abstract

Proteomes are well known to poorly correlate with transcriptomes measured from the same sample. While connected, the complex processes that impact the relationships between transcript and protein quantities remains an open research topic. Many studies have attempted to predict proteomes from transcriptomes with limited success. Here we use publicly available data from the Clinical Proteomics Tumor Analysis Consortium to show that deep learning models designed by neural architecture search (NAS) achieve improved prediction accuracy of proteome quantities from transcriptomics. We find that this benefit is largely due to including a residual connection in the architecture that allows input information to be remembered near the end of the network. Finally, we explore which groups of transcripts are functionally important for protein prediction using model interpretation with SHAP.

Identifiers

PMID39026798
PMCPMC11257616

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.