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Expression data of human tympanic membrane cells and epidermal keratinocytes [miRNA]

ABSTRACT: The data set compares the microRNA expression of two types of keratinocytes from the tympanic membrane and epidermis of the body. Healthy human samples were harvested for the analysis. Cells were cultivated to evaluate the effect of keratinocytes only. Few Chip Ids (11) were considered differentially expressed between the cell types. Six samples were analyzed in total. Each cell type in biological triplicates. Genes of p-value <0.05 and fold change of â¥ 1.5 were considered significant.

ORGANISM(S): Homo sapiens

SUBMITTER: Peder Aabel

PROVIDER: E-GEOD-76673 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Expression data of human tympanic membrane cells and epidermal keratinocytes

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Expression data of human tympanic membrane cells and epidermal keratinocytes

Project description:This SuperSeries is composed of the SubSeries listed below. Refer to individual Series

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Expression data of human tympanic membrane cells and epidermal keratinocytes [miRNA]

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Project description:Purpose: The goal of this study was to characterize the transcriptional response to injury of the murine tympanic membrane at multiple time points using single-cell RNA sequencing. Methods: mRNA profiles of Unwounded (Pars Tensa and Pars Flaccida) and Wounded (Day 1, Day 3, Day 7 and Day 14) murine tympanic membranes from WT FVB mice. The sequence reads that passed quality filters were analyzed at the transcript isoform level from fastq to matrix files using standard 10x genomics pipeline via CellRanger Results: Using the 10x Genomics Cell Ranger pipeline, we analyzed over 10,000 cells per timepoint from the UW and WO tympanic membranes, mapping the reads to the mouse genome (build mm10). The cells were then clustered primarily using the single-cell software package Seurat version 4. Conclusions: Our study represents the first detailed analysis of the regeneration timeline of the injured murine tympanic membrane, generated by RNA-seq technology. Our results show the emergence of novel populations on the tympanic membrane as it regenerates and characterizes the changes in all layers of the organ.

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