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Fast, sensitive and accurate integration of single-cell data with Harmony

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Hello, did someone tried to use Harmony on merged objects including more than 200 samples and more than 2 M cells? Which merging and normalization approach is suggested? And which...

hello harmony team, I wonder how to get the data set cell_lines from 10X data, I would be grateful if you can provide the detailed code of 10X data to...

Running the `RunHarmony(seuratobject)` with seurat 4.0.3 results in the following error ```Error in UseMethod(generic = "Key", object = object) : no applicable method for 'Key' applied to an object of...

Thanks for your tools! I met an error like this. And I can't found the harmony results. Error: (converted from warning) Invalid name supplied, making object name syntactically valid. New...

I have tried harmony for batch effect correction for my single-cell RNA-seq data to intergrate tumor and normal tissues, but when I used default parameter values, I found one problem...

Hi harmony group, I have a large gene expression matrix with 31734 genes by 147185 cells. As you can see from the screenshot below, running HarmonyMatrix() on the entire expression...

Hello Harmony team, I have a single cell RNA dataset with samples from 8 different tissues. The trouble I'm having is that some of these tissues were digested enzymatically, and...

I've been using Harmony for batch effect integration, but I would like to be able to continue downstream analysis in Seurat using the corrected data. I read [this review](https://genomebiology.biomedcentral.com/articles/10.1186/s13059-019-1850-9) rating...

Thanks for the tool! When I run RunHarmony I meet a warning :Warning: Invalid name supplied, making object name syntactically valid. New object name is Seurat..ProjectDim.RNA.harmony; see ?make.names for more...

Hi, Thank you so much for this great tool! Hope you can help me with this question. I am working with a scRNA-seq dataset in which I have been using...