2019
DOI: 10.1093/nar/gkz968
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FIN-Seq: transcriptional profiling of specific cell types from frozen archived tissue of the human central nervous system

Abstract: Thousands of frozen, archived tissue samples from the human central nervous system (CNS) are currently available in brain banks. As recent developments in RNA sequencing technologies are beginning to elucidate the cellular diversity present within the human CNS, it is becoming clear that an understanding of this diversity would greatly benefit from deeper transcriptional analyses. Single cell and single nucleus RNA profiling provide one avenue to decipher this heterogeneity. An alternative, complementary appro… Show more

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Cited by 14 publications
(12 citation statements)
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“…To capture the overall heterogeneity of infected and non-infected placenta samples, sampling, and biobanking criteria of different regions of placenta should be considered ( 135 ). Protocols are now available to use frozen tissue processed for single-cell/nuclei and spatial genomics ( 136 , 137 ). Hence, application of single-cell “omics” on infected vs. healthy human placental and decidual samples will enable us to evaluate cellular heterogeneity in response to infection.…”
Section: Challenges and Future Perspectivesmentioning
confidence: 99%
“…To capture the overall heterogeneity of infected and non-infected placenta samples, sampling, and biobanking criteria of different regions of placenta should be considered ( 135 ). Protocols are now available to use frozen tissue processed for single-cell/nuclei and spatial genomics ( 136 , 137 ). Hence, application of single-cell “omics” on infected vs. healthy human placental and decidual samples will enable us to evaluate cellular heterogeneity in response to infection.…”
Section: Challenges and Future Perspectivesmentioning
confidence: 99%
“…The cerebral cortex has diverged substantially during primate evolution, including molecular differences between corresponding cell types in different species 15,36,37 . Although a number of reports have profiled adult human pyramidal neurons to disentangle their transcriptional and epigenetic heterogeneity 38-40 , the molecular signatures of developing human PN subtypes are poorly defined. These are needed to investigate linkage to human disease, to allow cross-species comparative analysis, and for validation of the class identity of PN subtypes generated in vitro 41 .…”
Section: Resultsmentioning
confidence: 99%
“…However, due to the threshold of high-throughput scRNA-seq, profiling cell-type-specific gene expression is challenging. Comparisons between transcriptome analyses from purified cell populations have contributed additionally insightful molecular information about cortical cell subtypes ( Albert et al., 2017 ; Amamoto et al., 2020 ; Arlotta et al., 2005 ; Molyneaux et al., 2015 ; Pinto et al., 2008 ).…”
Section: Introductionmentioning
confidence: 99%