2020
DOI: 10.1186/s12987-020-00207-2
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Advancing brain barriers RNA sequencing: guidelines from experimental design to publication

Abstract: Background: RNA sequencing (RNA-Seq) in its varied forms has become an indispensable tool for analyzing differential gene expression and thus characterization of specific tissues. Aiming to understand the brain barriers genetic signature, RNA seq has also been introduced in brain barriers research. This has led to availability of both, bulk and single-cell RNA-Seq datasets over the last few years. If appropriately performed, the RNA-Seq studies provide powerful datasets that allow for significant deepening of … Show more

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Cited by 18 publications
(20 citation statements)
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“…The BBB is located at the level of microvascular endothelial cells in the CNS, which includes capillaries, pre-capillary arterioles and post-capillary venules ( Northrop and Yamamoto, 2015 ; Francisco et al, 2020 ). Previous gene profiling studies of brain vessels had several limitations, including the use of whole vessel fractions that contain many different cell types, the lack of description of the cerebral endothelial isolation procedures, and separation of the entire brain instead of specific areas ( Enerson and Drewes, 2006 ; Richard et al, 2010 ; Munji et al, 2019 ).…”
Section: Conclusion and Discussionmentioning
confidence: 99%
“…The BBB is located at the level of microvascular endothelial cells in the CNS, which includes capillaries, pre-capillary arterioles and post-capillary venules ( Northrop and Yamamoto, 2015 ; Francisco et al, 2020 ). Previous gene profiling studies of brain vessels had several limitations, including the use of whole vessel fractions that contain many different cell types, the lack of description of the cerebral endothelial isolation procedures, and separation of the entire brain instead of specific areas ( Enerson and Drewes, 2006 ; Richard et al, 2010 ; Munji et al, 2019 ).…”
Section: Conclusion and Discussionmentioning
confidence: 99%
“…Two biological replicates were analyzed of: HD180 iPSCs, HD180 iBMECs, HD-corrected iPSCs, and HD-corrected iBMECs. Given recent guidelines for RNA sequencing which suggest a minimum of three replicates [ 18 ], a limitation is that our analysis may be underpowered. iPSCs were harvested prior to differentiation in UM/F- media, while iBMECs were harvested as confluent monolayers 2 days following sub-culture on collagen IV and fibronectin-coated tissue-culture plates.…”
Section: Methodsmentioning
confidence: 99%
“…This function also reported an adjusted p-value (padj) based on the Benjamini-Hochberg procedure, which controls the false discovery rate (FDR). The threshold to identify DEGs was an adjusted p value ≤ 0.05 and a fold change (FC) ≥1.2, which has been reported as the optimal FC for nervous system transcriptomic analysis ( 45 ). A hierarchal clustering ( Figure 2 ) and a principle component analysis (PCA) ( Supplementary Figure 3 ) was performed on the differentially expressed set of genes to further evaluate and compare the transcription patterns between treatment conditions.…”
Section: Methodsmentioning
confidence: 99%