4 research outputs found
Supersymmetric dS/CFT
We put forward new explicit realisations of dS/CFT that relate
supersymmetric Euclidean vector models with reversed spin-statistics in three
dimensions to specific supersymmetric Vasiliev theories in four-dimensional de
Sitter space. The partition function of the free supersymmetric vector model
deformed by a range of low spin deformations that preserve supersymmetry
appears to specify a well-defined wave function with asymptotic de Sitter
boundary conditions in the bulk. In particular we find the wave function is
globally peaked at undeformed de Sitter space, with a low amplitude for strong
deformations. This suggests that supersymmetric de Sitter space is stable in
higher-spin gravity and in particular free from ghosts. We speculate this is a
limiting case of the de Sitter realizations in exotic string theories.Comment: V2: references and comments added, typos corrected, version published
in JHEP; 27 pages, 3 figures, 1 tabl
Additional file 5: Figure S5. of Massively parallel nanowell-based single-cell gene expression profiling
Percentage of mitochondrial transcripts plotted against total number of detected transcripts for mouse Ba/F3 cells (a), human cell lines (b), mouse cell lines (c), and pancreatic islets (d). Dashed lines indicate the minimum number of detected transcripts required as a cell QC filter for each data set. (PDF 409 kb
Additional file 4: Figure S4. of Massively parallel nanowell-based single-cell gene expression profiling
Heatmaps illustrating the total number of detected transcripts for each well selected for downstream processing. Data are for three microchips, each with 5184 wells arranged in a 72 × 72 square layout. Microchips 72,618 and 72,598 were used for profiling human and mouse cell lines (names of cell lines indicated in the plot). Microchip 72,625 was used for profiling pancreatic islets. For microchips with multiple dispensed samples, the dispense area for each sample is indicated. (PDF 93 kb
Additional file 2: Figure S2. of Massively parallel nanowell-based single-cell gene expression profiling
Checkerboard assay. (a) Image of a microchip where the right half contains negative control master mix (NTC wells, n = 2520) and the left half contains lambda DNA master mix master (Positive wells, n = 1024) and negative control master mix (Test wells, n = 1496) in a checkerboard pattern. (b) Number of Test wells with signal, number of NTC wells with signal, and calculated misalignment rate for 11 MSNDs and 19 microchips. (PDF 1288 kb