Loading…
scCRT: a contrastive-based dimensionality reduction model for scRNA-seq trajectory inference
Trajectory inference is a crucial task in single-cell RNA-sequencing downstream analysis, which can reveal the dynamic processes of biological development, including cell differentiation. Dimensionality reduction is an important step in the trajectory inference process. However, most existing trajec...
Saved in:
Published in: | Briefings in bioinformatics 2024-03, Vol.25 (3) |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | cdi_FETCH-LOGICAL-c284t-9e798a7b0862e5672e3ac9d07d6ebe10a4cc754e4ef05ca25c316616bbca8b193 |
container_end_page | |
container_issue | 3 |
container_start_page | |
container_title | Briefings in bioinformatics |
container_volume | 25 |
creator | Shi, Yuchen Wan, Jian Zhang, Xin Liang, Tingting Yin, Yuyu |
description | Trajectory inference is a crucial task in single-cell RNA-sequencing downstream analysis, which can reveal the dynamic processes of biological development, including cell differentiation. Dimensionality reduction is an important step in the trajectory inference process. However, most existing trajectory methods rely on cell features derived from traditional dimensionality reduction methods, such as principal component analysis and uniform manifold approximation and projection. These methods are not specifically designed for trajectory inference and fail to fully leverage prior information from upstream analysis, limiting their performance. Here, we introduce scCRT, a novel dimensionality reduction model for trajectory inference. In order to utilize prior information to learn accurate cells representation, scCRT integrates two feature learning components: a cell-level pairwise module and a cluster-level contrastive module. The cell-level module focuses on learning accurate cell representations in a reduced-dimensionality space while maintaining the cell-cell positional relationships in the original space. The cluster-level contrastive module uses prior cell state information to aggregate similar cells, preventing excessive dispersion in the low-dimensional space. Experimental findings from 54 real and 81 synthetic datasets, totaling 135 datasets, highlighted the superior performance of scCRT compared with commonly used trajectory inference methods. Additionally, an ablation study revealed that both cell-level and cluster-level modules enhance the model's ability to learn accurate cell features, facilitating cell lineage inference. The source code of scCRT is available at https://github.com/yuchen21-web/scCRT-for-scRNA-seq. |
doi_str_mv | 10.1093/bib/bbae204 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3050940473</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3050940473</sourcerecordid><originalsourceid>FETCH-LOGICAL-c284t-9e798a7b0862e5672e3ac9d07d6ebe10a4cc754e4ef05ca25c316616bbca8b193</originalsourceid><addsrcrecordid>eNo9kN9LwzAUhYMobk6ffJc8ClJ306RJ69sY_oKhMOabUJL0FjLaZks6Yf-9HZs-nXvgu-fhI-SWwSODgk-NM1NjNKYgzsiYCaUSAZk4P9xSJZmQfESuYlwDpKBydklGPFfABEvH5Dva-XL1RDW1vuuDjr37wcToiBWtXItddL7Tjev3NGC1s_1QaesrbGjtA412-TFLIm7p8LtG2_uwp66rMWBn8Zpc1LqJeHPKCfl6eV7N35LF5-v7fLZIbJqLPilQFblWBnKZYiZVilzbogJVSTTIQAtrVSZQYA2Z1WlmOZOSSWOszg0r-ITcH3c3wW93GPuyddFi0-gO_S6WHDIoBAjFB_ThiNrgYwxYl5vgWh32JYPyoLMcdJYnnQN9dxremRarf_bPH_8F9URygA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3050940473</pqid></control><display><type>article</type><title>scCRT: a contrastive-based dimensionality reduction model for scRNA-seq trajectory inference</title><source>PubMed (Medline)</source><source>Oxford Open</source><source>BSC - Ebsco (Business Source Ultimate)</source><creator>Shi, Yuchen ; Wan, Jian ; Zhang, Xin ; Liang, Tingting ; Yin, Yuyu</creator><creatorcontrib>Shi, Yuchen ; Wan, Jian ; Zhang, Xin ; Liang, Tingting ; Yin, Yuyu</creatorcontrib><description>Trajectory inference is a crucial task in single-cell RNA-sequencing downstream analysis, which can reveal the dynamic processes of biological development, including cell differentiation. Dimensionality reduction is an important step in the trajectory inference process. However, most existing trajectory methods rely on cell features derived from traditional dimensionality reduction methods, such as principal component analysis and uniform manifold approximation and projection. These methods are not specifically designed for trajectory inference and fail to fully leverage prior information from upstream analysis, limiting their performance. Here, we introduce scCRT, a novel dimensionality reduction model for trajectory inference. In order to utilize prior information to learn accurate cells representation, scCRT integrates two feature learning components: a cell-level pairwise module and a cluster-level contrastive module. The cell-level module focuses on learning accurate cell representations in a reduced-dimensionality space while maintaining the cell-cell positional relationships in the original space. The cluster-level contrastive module uses prior cell state information to aggregate similar cells, preventing excessive dispersion in the low-dimensional space. Experimental findings from 54 real and 81 synthetic datasets, totaling 135 datasets, highlighted the superior performance of scCRT compared with commonly used trajectory inference methods. Additionally, an ablation study revealed that both cell-level and cluster-level modules enhance the model's ability to learn accurate cell features, facilitating cell lineage inference. The source code of scCRT is available at https://github.com/yuchen21-web/scCRT-for-scRNA-seq.</description><identifier>ISSN: 1467-5463</identifier><identifier>ISSN: 1477-4054</identifier><identifier>EISSN: 1477-4054</identifier><identifier>DOI: 10.1093/bib/bbae204</identifier><identifier>PMID: 38701412</identifier><language>eng</language><publisher>England</publisher><subject>Algorithms ; Computational Biology - methods ; RNA-Seq - methods ; Single-Cell Gene Expression Analysis - methods ; Software</subject><ispartof>Briefings in bioinformatics, 2024-03, Vol.25 (3)</ispartof><rights>The Author(s) 2024. Published by Oxford University Press.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c284t-9e798a7b0862e5672e3ac9d07d6ebe10a4cc754e4ef05ca25c316616bbca8b193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38701412$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shi, Yuchen</creatorcontrib><creatorcontrib>Wan, Jian</creatorcontrib><creatorcontrib>Zhang, Xin</creatorcontrib><creatorcontrib>Liang, Tingting</creatorcontrib><creatorcontrib>Yin, Yuyu</creatorcontrib><title>scCRT: a contrastive-based dimensionality reduction model for scRNA-seq trajectory inference</title><title>Briefings in bioinformatics</title><addtitle>Brief Bioinform</addtitle><description>Trajectory inference is a crucial task in single-cell RNA-sequencing downstream analysis, which can reveal the dynamic processes of biological development, including cell differentiation. Dimensionality reduction is an important step in the trajectory inference process. However, most existing trajectory methods rely on cell features derived from traditional dimensionality reduction methods, such as principal component analysis and uniform manifold approximation and projection. These methods are not specifically designed for trajectory inference and fail to fully leverage prior information from upstream analysis, limiting their performance. Here, we introduce scCRT, a novel dimensionality reduction model for trajectory inference. In order to utilize prior information to learn accurate cells representation, scCRT integrates two feature learning components: a cell-level pairwise module and a cluster-level contrastive module. The cell-level module focuses on learning accurate cell representations in a reduced-dimensionality space while maintaining the cell-cell positional relationships in the original space. The cluster-level contrastive module uses prior cell state information to aggregate similar cells, preventing excessive dispersion in the low-dimensional space. Experimental findings from 54 real and 81 synthetic datasets, totaling 135 datasets, highlighted the superior performance of scCRT compared with commonly used trajectory inference methods. Additionally, an ablation study revealed that both cell-level and cluster-level modules enhance the model's ability to learn accurate cell features, facilitating cell lineage inference. The source code of scCRT is available at https://github.com/yuchen21-web/scCRT-for-scRNA-seq.</description><subject>Algorithms</subject><subject>Computational Biology - methods</subject><subject>RNA-Seq - methods</subject><subject>Single-Cell Gene Expression Analysis - methods</subject><subject>Software</subject><issn>1467-5463</issn><issn>1477-4054</issn><issn>1477-4054</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNo9kN9LwzAUhYMobk6ffJc8ClJ306RJ69sY_oKhMOabUJL0FjLaZks6Yf-9HZs-nXvgu-fhI-SWwSODgk-NM1NjNKYgzsiYCaUSAZk4P9xSJZmQfESuYlwDpKBydklGPFfABEvH5Dva-XL1RDW1vuuDjr37wcToiBWtXItddL7Tjev3NGC1s_1QaesrbGjtA412-TFLIm7p8LtG2_uwp66rMWBn8Zpc1LqJeHPKCfl6eV7N35LF5-v7fLZIbJqLPilQFblWBnKZYiZVilzbogJVSTTIQAtrVSZQYA2Z1WlmOZOSSWOszg0r-ITcH3c3wW93GPuyddFi0-gO_S6WHDIoBAjFB_ThiNrgYwxYl5vgWh32JYPyoLMcdJYnnQN9dxremRarf_bPH_8F9URygA</recordid><startdate>20240327</startdate><enddate>20240327</enddate><creator>Shi, Yuchen</creator><creator>Wan, Jian</creator><creator>Zhang, Xin</creator><creator>Liang, Tingting</creator><creator>Yin, Yuyu</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240327</creationdate><title>scCRT: a contrastive-based dimensionality reduction model for scRNA-seq trajectory inference</title><author>Shi, Yuchen ; Wan, Jian ; Zhang, Xin ; Liang, Tingting ; Yin, Yuyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c284t-9e798a7b0862e5672e3ac9d07d6ebe10a4cc754e4ef05ca25c316616bbca8b193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Algorithms</topic><topic>Computational Biology - methods</topic><topic>RNA-Seq - methods</topic><topic>Single-Cell Gene Expression Analysis - methods</topic><topic>Software</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shi, Yuchen</creatorcontrib><creatorcontrib>Wan, Jian</creatorcontrib><creatorcontrib>Zhang, Xin</creatorcontrib><creatorcontrib>Liang, Tingting</creatorcontrib><creatorcontrib>Yin, Yuyu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Briefings in bioinformatics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shi, Yuchen</au><au>Wan, Jian</au><au>Zhang, Xin</au><au>Liang, Tingting</au><au>Yin, Yuyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>scCRT: a contrastive-based dimensionality reduction model for scRNA-seq trajectory inference</atitle><jtitle>Briefings in bioinformatics</jtitle><addtitle>Brief Bioinform</addtitle><date>2024-03-27</date><risdate>2024</risdate><volume>25</volume><issue>3</issue><issn>1467-5463</issn><issn>1477-4054</issn><eissn>1477-4054</eissn><abstract>Trajectory inference is a crucial task in single-cell RNA-sequencing downstream analysis, which can reveal the dynamic processes of biological development, including cell differentiation. Dimensionality reduction is an important step in the trajectory inference process. However, most existing trajectory methods rely on cell features derived from traditional dimensionality reduction methods, such as principal component analysis and uniform manifold approximation and projection. These methods are not specifically designed for trajectory inference and fail to fully leverage prior information from upstream analysis, limiting their performance. Here, we introduce scCRT, a novel dimensionality reduction model for trajectory inference. In order to utilize prior information to learn accurate cells representation, scCRT integrates two feature learning components: a cell-level pairwise module and a cluster-level contrastive module. The cell-level module focuses on learning accurate cell representations in a reduced-dimensionality space while maintaining the cell-cell positional relationships in the original space. The cluster-level contrastive module uses prior cell state information to aggregate similar cells, preventing excessive dispersion in the low-dimensional space. Experimental findings from 54 real and 81 synthetic datasets, totaling 135 datasets, highlighted the superior performance of scCRT compared with commonly used trajectory inference methods. Additionally, an ablation study revealed that both cell-level and cluster-level modules enhance the model's ability to learn accurate cell features, facilitating cell lineage inference. The source code of scCRT is available at https://github.com/yuchen21-web/scCRT-for-scRNA-seq.</abstract><cop>England</cop><pmid>38701412</pmid><doi>10.1093/bib/bbae204</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1467-5463 |
ispartof | Briefings in bioinformatics, 2024-03, Vol.25 (3) |
issn | 1467-5463 1477-4054 1477-4054 |
language | eng |
recordid | cdi_proquest_miscellaneous_3050940473 |
source | PubMed (Medline); Oxford Open; BSC - Ebsco (Business Source Ultimate) |
subjects | Algorithms Computational Biology - methods RNA-Seq - methods Single-Cell Gene Expression Analysis - methods Software |
title | scCRT: a contrastive-based dimensionality reduction model for scRNA-seq trajectory inference |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-29T13%3A53%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=scCRT:%20a%20contrastive-based%20dimensionality%20reduction%20model%20for%20scRNA-seq%20trajectory%20inference&rft.jtitle=Briefings%20in%20bioinformatics&rft.au=Shi,%20Yuchen&rft.date=2024-03-27&rft.volume=25&rft.issue=3&rft.issn=1467-5463&rft.eissn=1477-4054&rft_id=info:doi/10.1093/bib/bbae204&rft_dat=%3Cproquest_cross%3E3050940473%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c284t-9e798a7b0862e5672e3ac9d07d6ebe10a4cc754e4ef05ca25c316616bbca8b193%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3050940473&rft_id=info:pmid/38701412&rfr_iscdi=true |