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I am analyzing a 10X single cell multiome datasets carried out in 3ctrl and 3 treated cell linds, after running standard cellranger pipeline for generating counts file and atac fragments.
I am wondering how to analyze them together or i have to analyze one by one like ctrl_1 , then ctrl_2 and then ctrl_3. same for treated.
Because I want to link peaks to genes and i want to show two heat maps, one as average of Ctrl and one as average of treated.
This discussion was converted from issue #1895 on January 31, 2025 02:41.
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I am analyzing a 10X single cell multiome datasets carried out in 3ctrl and 3 treated cell linds, after running standard cellranger pipeline for generating counts file and atac fragments.
I am wondering how to analyze them together or i have to analyze one by one like ctrl_1 , then ctrl_2 and then ctrl_3. same for treated.
Because I want to link peaks to genes and i want to show two heat maps, one as average of Ctrl and one as average of treated.
Please guide.
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