Closed brianherb closed 3 years ago
Looks very nice, Brian! Just what I'd hoped we could produce for the MERFISH data. I agree that dots (not cell shapes) at the appropriate x,y position is just fine. However, I do wonder if the interpretation would it be made easier by producing drawings that simply show the inferred boundaries between layers and other major subdivisions.
The other visualization that I could potentially imagine creating would be an "imputed" version, integrating data from MERFISH and scRNA-seq. Specifically, I'm trying to think how one could get the MERFISH profile to show information about all the genes, not just the 250 that they imaged. Since the cells in the MERFISH and 10x datasets are given the same cell type assignments, would it be useful to assign each cell an expression level for every gene based on the median value for that cell type in the 10x data?
this looks VERY cool guys! next time there is a discussion/demo/anything on this, i'd love to join and get more involved in the BICCN work and profiles. i think we could add very valuable perspectives on this and more BICCN data using our gene lists and projection across space in these contexts, carlo
On Thu, Aug 20, 2020 at 9:26 AM Seth Ament notifications@github.com wrote:
Looks very nice, Brian! Just what I'd hoped we could produce for the MERFISH data. I agree that dots (not cell shapes) at the appropriate x,y position is just fine. However, I do wonder if the interpretation would it be made easier by producing drawings that simply show the inferred boundaries between layers and other major subdivisions.
The other visualization that I could potentially imagine creating would be an "imputed" version, integrating data from MERFISH and scRNA-seq. Specifically, I'm trying to think how one could get the MERFISH profile to show information about all the genes, not just the 250 that they imaged. Since the cells in the MERFISH and 10x datasets are given the same cell type assignments, would it be useful to assign each cell an expression level for every gene based on the median value for that cell type in the 10x data?
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-- Carlo
Im listening to this mornings meeting where you guys discuss this. given that the data format and display parameters are nearly identical to the [sc]RNAseq data in NeMO, the gene lists and projection should require no extra engineering once implemented for "conventional" RNAseq etc in NeMO. for example - a transcriptional dimension from bulk in vitro organoid RNAseq data could be projected into MERfish data and light up particular layer-specific neurons in vivo, giving a precise perspective on what elements of in vivo development are recapitulated in vitro - super-exciting. carlo
On Fri, Aug 21, 2020 at 1:14 PM Carlo Colantuoni colantuonicarlo@gmail.com wrote:
this looks VERY cool guys! next time there is a discussion/demo/anything on this, i'd love to join and get more involved in the BICCN work and profiles. i think we could add very valuable perspectives on this and more BICCN data using our gene lists and projection across space in these contexts, carlo
On Thu, Aug 20, 2020 at 9:26 AM Seth Ament notifications@github.com wrote:
Looks very nice, Brian! Just what I'd hoped we could produce for the MERFISH data. I agree that dots (not cell shapes) at the appropriate x,y position is just fine. However, I do wonder if the interpretation would it be made easier by producing drawings that simply show the inferred boundaries between layers and other major subdivisions.
The other visualization that I could potentially imagine creating would be an "imputed" version, integrating data from MERFISH and scRNA-seq. Specifically, I'm trying to think how one could get the MERFISH profile to show information about all the genes, not just the 250 that they imaged. Since the cells in the MERFISH and 10x datasets are given the same cell type assignments, would it be useful to assign each cell an expression level for every gene based on the median value for that cell type in the 10x data?
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-- Carlo
-- Carlo
Made a test profile, but had to do it on gEAR - here are some screen shots:
Patchseq -
@jorvis - the attached IT_test.zip file contains two files - a svg (IT_test.svg) and a data matrix (ITexpression.csv). The goal is to color the rectangles at the bottom of the image like a heatmap reflecting the expression from the data matrix.
This looks awesome, Brian!
yes it does look great!!
On Tue, Oct 6, 2020 at 5:20 PM Seth Ament notifications@github.com wrote:
This looks awesome, Brian!
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-- Carlo
Can you please attach a screenshot?
On Tue, Oct 6, 2020 at 10:05 PM Carlo Colantuoni notifications@github.com wrote:
yes it does look great!!
On Tue, Oct 6, 2020 at 5:20 PM Seth Ament notifications@github.com wrote:
This looks awesome, Brian!
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.
-- Carlo
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@hertzron - Seth and Carlo were reacting to this mock-up:
This image is to be loaded for dataset ID: 403cf3ea-c5cb-7add-3142-a96945152f63
Sorry, I see you referenced this in #138
Profile completed
Merfish - Looking at the data, we actually have enough to make good looking plots. The actual experiment involved 2 mice - and they imaged 30 coronal slices per mouse (probing for 258 genes). For each slice, we have the xy position, size and cell type for each cell. The attached plots reproduce flagship figure 3d which looks at just the IT neurons (flagship figure: https://drive.google.com/drive/folders/1fFM1AnKbq0o0PXRZTRxlqiZuOS7g_YTt.) Each plot is a different slice and I sized the points on the plot relative to the cell volume. There is also a corresponding counts matrix for the ~300,000 cells and 254 genes, but I am having difficulty matching the cell ids.
The major difference is that we don't have the actual images, so the cells are depicted as circles instead of true cell outlines, but I feel like this is good enough, and might make plotting a lot easier. (seems like a lot of work to produce 60 SVG's too)