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Statistical Analysis Supports Pervasive RNA Subcellular Localization and Alternative UTR Regulation- [electronic resource]
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.
- Subject Added Entry-Topical Term
- Neurons.
- Subject Added Entry-Topical Term
- Cytoskeleton.
- Subject Added Entry-Topical Term
- Regulation.
- Subject Added Entry-Topical Term
- 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.
- Subject Added Entry-Topical Term
- Dissection.
- Subject Added Entry-Topical Term
- Morphology.
- Subject Added Entry-Topical Term
- Motility.
- Subject Added Entry-Topical Term
- 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
- 로그인을 한후 보실 수 있는 자료입니다.
- Control Number
- joongbu:643222