This graph displays the expression value in rpkm for each cell type in the midgut. The expression values originate from RNA sequencing realized on FACS sorted cell populations from the midgut.
ISC: intestinal stem cell (delta-Gal4>UAS-GFP), EB: enteroblast (Su(H)-Gal4>UAS-GFP), EC: enterocyte (Myo1A-Gal4>UAS-GFP), EE: enteroendocrine cell (prosperov1-Gal4>UAS-GFP), VM: visceral muscle (how-Gal4>UAS-GFP)

This section displays rpkm values for each region and all cell types. The second graph is only displayed when one gene is searched. All cell types and regions are displayed in one single graph for easy comparison.

These graphs display the expression value in rpkm for each region in each cell type along the midgut. The expression values originate from RNA sequencing realized on FACS sorted cell populations from dissected regions of the midgut.
ISC: intestinal stem cell (delta-Gal4>UAS-GFP), EB: enteroblast (Su(H)-Gal4>UAS-GFP), EC: enterocyte (Myo1A-Gal4>UAS-GFP), EE: enteroendocrine cell (prosperov1-Gal4>UAS-GFP), VM: visceral muscle (how-Gal4>UAS-GFP)
Regions are ordered from anterior (R1) to posterior (R5) and described elsewhere (Buchon et al, 2013, Cell reports).

This graph displays the fold enrichment for each gene in each cell type in response to infection with the entomopathogenic bacteria Pseudomonas entomophila (Pe). The values originate from RNA sequencing realized on FACS sorted cell populations from whole midguts either unchallenged or infected with Pe. Flies were starved for 2 hrs and then infected for 48hrs with P.entomophila bacteria on filter paper. Cell populations were then isolated using FACS (based on size and cell type specific marker expression).