Evidence map›Paper›PMID 39192845›Full record

ArticlePNAS nexus2024

Raman spectroscopic deep learning with signal aggregated representations for enhanced cell phenotype and signature identification.

Songlin Lu, Yuanfang Huang, Wan Xiang Shen, Yu Lin Cao, Mengna Cai, Yan Chen, Ying Tan, Yu Yang Jiang, Yu Zong Chen

Abstract read
In one paragraph

Article in PNAS nexus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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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

9 authors.

Songlin LuThe State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Biology, Tsinghua Shenzhen International Graduate School, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.ORCID https://orcid.org/0000-0003-1440-3938
Yuanfang HuangThe State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Biology, Tsinghua Shenzhen International Graduate School, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.ORCID https://orcid.org/0000-0003-2312-317X
Wan Xiang ShenBioinformatics and Drug Design Group, Department of Pharmacy, National University of Singapore, 18 Science Drive 4, Singapore 117543, Singapore.ORCID https://orcid.org/0000-0001-7114-3664
Yu Lin CaoTangyi and Tsinghua Shenzhen International Graduate School Collaborative Program, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.
Mengna CaiTangyi and Tsinghua Shenzhen International Graduate School Collaborative Program, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.
Yan ChenThe State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Biology, Tsinghua Shenzhen International Graduate School, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.ORCID https://orcid.org/0000-0002-9332-8165
Ying TanThe State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Biology, Tsinghua Shenzhen International Graduate School, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.ORCID https://orcid.org/0000-0003-2957-0165
Yu Yang JiangSchool of Pharmaceutical Sciences, Tsinghua University, 30 Shuangqing Road, Haidian District, Beijing 100084, P. R. China.
Yu Zong ChenThe State Key Laboratory of Chemical Oncogenomics, Key Laboratory of Chemical Biology, Tsinghua Shenzhen International Graduate School, Tsinghua University, 2279 Lishui Road, Nanshan District, Shenzhen 518055, Guangdong, P. R. China.ORCID https://orcid.org/0000-0002-5473-8022

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Feature representation is critical for data learning, particularly in learning spectroscopic data. Machine learning (ML) and deep learning (DL) models learn Raman spectra for rapid, nondestructive, and label-free cell phenotype identification, which facilitate diagnostic, therapeutic, forensic, and microbiological applications. But these are challenged by high-dimensional, unordered, and low-sample spectroscopic data. Here, we introduced novel 2D image-like dual signal and component aggregated representations by restructuring Raman spectra and principal components, which enables spectroscopic DL for enhanced cell phenotype and signature identification. New ConvNet models DSCARNets significantly outperformed the state-of-the-art (SOTA) ML and DL models on six benchmark datasets, mostly with >2% improvement over the SOTA performance of 85-97% accuracies. DSCARNets also performed well on four additional datasets against SOTA models of extremely high performances (>98%) and two datasets without a published supervised phenotype classification model. Explainable DSCARNets identified Raman signatures consistent with experimental indications.

Indexed as

cell phenotypingdeep learningfeature representationRaman signature identificationRaman spectra

Identifiers

PMID39192845
PMCPMC11348106

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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.