<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Imoto Y</submitter><funding>AMED-CREST</funding><funding>JST PREST</funding><funding>JSPS Grant-in-Aid for Specially Promoted Research</funding><funding>MEXT Grant-in-Aid for Transformative Research Areas B</funding><funding>JSPS Grant-in-Aid for Early-Career Scientists</funding><funding>JST MIRAI Program Grant</funding><funding>World Premier International Research Center Initiative</funding><funding>JST CREST Mathematics Grant</funding><pagination>e202201591</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9363502</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(12)</volume><pubmed_abstract>Single-cell RNA sequencing (scRNA-seq) can determine gene expression in numerous individual cells simultaneously, promoting progress in the biomedical sciences. However, scRNA-seq data are high-dimensional with substantial technical noise, including dropouts. During analysis of scRNA-seq data, such noise engenders a statistical problem known as the curse of dimensionality (COD). Based on high-dimensional statistics, we herein formulate a noise reduction method, RECODE (resolution of the curse of dimensionality), for high-dimensional data with random sampling noise. We show that RECODE consistently resolves COD in relevant scRNA-seq data with unique molecular identifiers. RECODE does not involve dimension reduction and recovers expression values for all genes, including lowly expressed gene</pubmed_abstract><journal>Life science alliance</journal><pubmed_title>Resolution of the curse of dimensionality in single-cell RNA sequencing data analysis.</pubmed_title><pmcid>PMC9363502</pmcid><funding_grant_id>22682401</funding_grant_id><funding_grant_id>JPMJPR2021</funding_grant_id><funding_grant_id>JP19gm1310002h</funding_grant_id><funding_grant_id>20H05761</funding_grant_id><funding_grant_id>15656429</funding_grant_id><funding_grant_id>22H04920</funding_grant_id><funding_grant_id>17H06098</funding_grant_id><funding_grant_id>18K14714</funding_grant_id><pubmed_authors>Imoto Y</pubmed_authors><pubmed_authors>Escolar EG</pubmed_authors><pubmed_authors>Yabuta Y</pubmed_authors><pubmed_authors>Kojima Y</pubmed_authors><pubmed_authors>Yamamoto T</pubmed_authors><pubmed_authors>Yoshiwaki M</pubmed_authors><pubmed_authors>Nakamura T</pubmed_authors><pubmed_authors>Hiraoka Y</pubmed_authors><pubmed_authors>Katou Y</pubmed_authors><pubmed_authors>Saitou M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Resolution of the curse of dimensionality in single-cell RNA sequencing data analysis.</name><description>Single-cell RNA sequencing (scRNA-seq) can determine gene expression in numerous individual cells simultaneously, promoting progress in the biomedical sciences. However, scRNA-seq data are high-dimensional with substantial technical noise, including dropouts. During analysis of scRNA-seq data, such noise engenders a statistical problem known as the curse of dimensionality (COD). Based on high-dimensional statistics, we herein formulate a noise reduction method, RECODE (resolution of the curse of dimensionality), for high-dimensional data with random sampling noise. We show that RECODE consistently resolves COD in relevant scRNA-seq data with unique molecular identifiers. RECODE does not involve dimension reduction and recovers expression values for all genes, including lowly expressed gene</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2026-05-09T19:35:08.342Z</modification><creation>2025-04-21T14:49:14.43Z</creation></dates><accession>S-EPMC9363502</accession><cross_references><pubmed>35944930</pubmed><doi>10.26508/lsa.202201591</doi></cross_references></HashMap>