QuantISH: RNA in situ hybridization image analysis framework for quantifying cell type-specific target RNA expression and variability

dc.contributor.authorJamalzadeh Sanaz
dc.contributor.authorHäkkinen Antti
dc.contributor.authorAndersson Noora
dc.contributor.authorHuhtinen Kaisa
dc.contributor.authorLaury Anna
dc.contributor.authorHietanen Sakari
dc.contributor.authorHynninen Johanna
dc.contributor.authorOikkonen Jaana
dc.contributor.authorCarpén Olli
dc.contributor.authorVirtanen Anni
dc.contributor.authorHautaniemi Sampsa
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=synnytys- ja naistentautioppi|en=Obstetrics and Gynaecology|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.74725736230
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.contributor.organization-code2607100
dc.converis.publication-id174843147
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/174843147
dc.date.accessioned2022-10-28T14:04:17Z
dc.date.available2022-10-28T14:04:17Z
dc.description.abstractRNA in situ hybridization (RNA-ISH) is a powerful spatial transcriptomics technology to characterize target RNA abundance and localization in individual cells. This allows analysis of tumor heterogeneity and expression localization, which are not readily obtainable through transcriptomic data analysis. RNA-ISH experiments produce large amounts of data and there is a need for automated analysis methods. Here we present QuantISH, a comprehensive open-source RNA-ISH image analysis pipeline that quantifies marker expressions in individual carcinoma, immune, and stromal cells on chromogenic or fluorescent in situ hybridization images. QuantISH is designed to be modular and can be adapted to various image and sample types and staining protocols. We show that in chromogenic RNA in situ hybridization images of high-grade serous carcinoma (HGSC) QuantISH cancer cell classification has high precision, and signal expression quantification is in line with visual assessment. We further demonstrate the power of QuantISH by showing that CCNE1 average expression and DDIT3 expression variability, as captured by the variability factor developed herein, act as candidate biomarkers in HGSC. Altogether, our results demonstrate that QuantISH can quantify RNA expression levels and their variability in carcinoma cells, and thus paves the way to utilize RNA-ISH technology.
dc.identifier.eissn1530-0307
dc.identifier.jour-issn0023-6837
dc.identifier.olddbid186087
dc.identifier.oldhandle10024/169181
dc.identifier.urihttps://www.utupub.fi/handle/11111/42888
dc.identifier.urlhttps://www.nature.com/articles/s41374-022-00743-5
dc.identifier.urnURN:NBN:fi-fe2022081154804
dc.language.isoen
dc.okm.affiliatedauthorHuhtinen, Kaisa
dc.okm.affiliatedauthorHietanen, Sakari
dc.okm.affiliatedauthorHynninen, Johanna
dc.okm.affiliatedauthorCarpen, Olli
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherSPRINGERNATURE
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.doi10.1038/s41374-022-00743-5
dc.relation.ispartofjournalLaboratory Investigation
dc.source.identifierhttps://www.utupub.fi/handle/10024/169181
dc.titleQuantISH: RNA in situ hybridization image analysis framework for quantifying cell type-specific target RNA expression and variability
dc.year.issued2022

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