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David Zemmour
Aug 19, 2022
In ImmGen-T Forum
Let's say we are sequencing total CD3+ cells in a tissue, and my population of interest is rare, i.e., 1%. How many cells should I sequence and have enough of my rare cell population? This is a power analysis. I will refer you to this helpful online tool by Satija's lab: https://satijalab.org/howmanycells/ For example, if tetramer+ cells are 1% of my CD3+ T cells and we want to sequence at least 20 cells, we need about 3,000 cells to have a ~95% chance of capturing 20 tetramer+ cells.
How many cells should I sequence? content media
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David Zemmour
Jun 20, 2022
In ImmGen-T Forum
1. Make sure they are represented in enough numbers (pool mice, enrich, etc.). 2. In the spirit of profiling all T cells in ImmGen T, we would also suggest profiling all CD3+ cells as one of the samples. Will serve as reference of the range of states that cells can adopt, background repertoire analysis, etc. 3. Don't forget the spleen whole CD45+ control when you plan the experiment and fill the sample prep excel sheet.
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David Zemmour
Jun 20, 2022
In ImmGen-T Forum
Here is the Rosetta viewer! We deposited recent T cell profiling by CITE-seq from baseline tissues. Please be patient with Rosetta, work in progress! Please allow 10-30s for the data to load before selecting samples. https://cbdm.connect.hms.harvard.edu/Rosetta_ImmGenT/
Rosetta viewer content media
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David Zemmour
Apr 25, 2022
In ImmGen-T Forum
I understand that you will use a CITE-seq panel. What is the list of antibodies pooled in the panel?
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