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Statistical Analysis Supports Pervasive RNA Subcellular Localization and Alternative UTR Regulation- [electronic resource]
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Statistical Analysis Supports Pervasive RNA Subcellular Localization and Alternative UTR Regulation- [electronic resource]
자료유형  
 학위논문
Control Number  
0016931986
International Standard Book Number  
9798379654320
Dewey Decimal Classification Number  
591
Main Entry-Personal Name  
Bierman, Robert Forrest.
Publication, Distribution, etc. (Imprint  
[S.l.] : Stanford University., 2023
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2023
Physical Description  
1 online resource(101 p.)
General Note  
Source: Dissertations Abstracts International, Volume: 84-12, Section: B.
General Note  
Advisor: Harbury, Pehr;Krasnow, Mark;Salzman, Julia.
Dissertation Note  
Thesis (Ph.D.)--Stanford University, 2023.
Restrictions on Access Note  
This item must not be sold to any third party vendors.
Summary, Etc.  
요약Understanding the subcellular localization of RNA molecules across different cell-types and tissues provides a window into previously unknown biology and disease. Low-plex RNA imaging technologies, where only a handful of RNA species could be observed in a single experiment, have been transformed by novel spatially resolved imaging and sequencing techniques which can simultaneously investigate thousands of genes. Named "Method of the Year" in 2019 by Nature Methods, the field of spatially resolved transcriptomics continues to accelerate in resolution, sensitivity, and ease of use. Large and exciting datasets have been produced from these efforts, but have been underutilized to discover subcellular RNA localization.We introduce a novel statistical framework to identify RNA subcellular localization patterns in publicly available datasets. We detect that a majority of investigated genes have non-random RNA distribution, and often differential distribution between cell-types.We've combined our analyses of spatial datasets with standard, spatially-naive, single-cell RNA sequencing to further identify genes which have subcellular localization patterning correlated with RNA isoform usage to generate testable hypotheses which we've collaborated with others to successfully validate.Spatial Transcriptomics is rapidly evolving, and we expect that our contribution of a flexible and statistically-sound algorithm will be applicable for the impending influx of spatial datasets.
Subject Added Entry-Topical Term  
Embryos.
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Neurons.
Subject Added Entry-Topical Term  
Cytoskeleton.
Subject Added Entry-Topical Term  
Regulation.
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Fibroblasts.
Subject Added Entry-Topical Term  
Binding sites.
Subject Added Entry-Topical Term  
Microscopy.
Subject Added Entry-Topical Term  
Medical research.
Subject Added Entry-Topical Term  
Insects.
Subject Added Entry-Topical Term  
Localization.
Subject Added Entry-Topical Term  
Genes.
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Dissection.
Subject Added Entry-Topical Term  
Morphology.
Subject Added Entry-Topical Term  
Motility.
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Cell culture.
Subject Added Entry-Topical Term  
Cellular biology.
Subject Added Entry-Topical Term  
Medicine.
Added Entry-Corporate Name  
Stanford University.
Host Item Entry  
Dissertations Abstracts International. 84-12B.
Host Item Entry  
Dissertation Abstract International
Electronic Location and Access  
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Control Number  
joongbu:643222
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