|
|
|
|
LEADER |
01986 am a22002533u 4500 |
001 |
105746 |
042 |
|
|
|a dc
|
100 |
1 |
0 |
|a Satija, Rahul
|e author
|
100 |
1 |
0 |
|a Massachusetts Institute of Technology. Department of Biology
|e contributor
|
100 |
1 |
0 |
|a Regev, Aviv
|e contributor
|
700 |
1 |
0 |
|a Farrell, Jeffrey A
|e author
|
700 |
1 |
0 |
|a Gennert, David
|e author
|
700 |
1 |
0 |
|a Schier, Alexander F
|e author
|
700 |
1 |
0 |
|a Regev, Aviv
|e author
|
245 |
0 |
0 |
|a Spatial reconstruction of single-cell gene expression data
|
260 |
|
|
|b Nature Publishing Group,
|c 2016-12-07T20:58:05Z.
|
856 |
|
|
|z Get fulltext
|u http://hdl.handle.net/1721.1/105746
|
520 |
|
|
|a Spatial localization is a key determinant of cellular fate and behavior, but methods for spatially resolved, transcriptome-wide gene expression profiling across complex tissues are lacking. RNA staining methods assay only a small number of transcripts, whereas single-cell RNA-seq, which measures global gene expression, separates cells from their native spatial context. Here we present Seurat, a computational strategy to infer cellular localization by integrating single-cell RNA-seq data with in situ RNA patterns. We applied Seurat to spatially map 851 single cells from dissociated zebrafish (Danio rerio) embryos and generated a transcriptome-wide map of spatial patterning. We confirmed Seurat's accuracy using several experimental approaches, then used the strategy to identify a set of archetypal expression patterns and spatial markers. Seurat correctly localizes rare subpopulations, accurately mapping both spatially restricted and scattered groups. Seurat will be applicable to mapping cellular localization within complex patterned tissues in diverse systems.
|
520 |
|
|
|a Howard Hughes Medical Institute
|
520 |
|
|
|a Klarman Cell Observatory
|
520 |
|
|
|a National Human Genome Research Institute (U.S.) (Centers for Excellence in Genomics Science 1P50HG006193)
|
546 |
|
|
|a en_US
|
655 |
7 |
|
|a Article
|
773 |
|
|
|t Nature Biotechnology
|