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Thank you for this SCEVAN tool which I use a lot at the moment,
I am analysing merged datasets to investigate patient-specificity among CNV subclones. However, using a merged dataset of 24 donors, generating 12 subclones, there was an error at the end of the analysis pipeline. How should I interpret this error? Is there a maximum to the amount of subclones that can be analyzed (9)?
Thanks in advance!
The text was updated successfully, but these errors were encountered:
I am also curious about this. I am analyzing two samples from the same patient (taken at different times). With these datasets merged in datasets from 2 healthy donors (P1 + H1/H2, P2 + H1/H2, P1+P2+H1/H2), and specified these as the healthy cells. When I do these 3 runs, the number of subclones produce from the runs on the individual datasets are more than the number of subclones from the runs on the merged dataset.
@augjensen wondering if you managed to figure out this issue?I'm facing the same error when merging samples however it works fine when running the pipeline on individual samples.
Thank you for this SCEVAN tool which I use a lot at the moment,
I am analysing merged datasets to investigate patient-specificity among CNV subclones. However, using a merged dataset of 24 donors, generating 12 subclones, there was an error at the end of the analysis pipeline. How should I interpret this error? Is there a maximum to the amount of subclones that can be analyzed (9)?
Thanks in advance!
The text was updated successfully, but these errors were encountered: