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dds = DeseqDataSet(counts=test_gene_expression_df, metadata=test_metadata_df,design_factors="Cluster") dds.deseq2()
Let me know if you need to look at the counts and metadata dataframes.
@mohammedali452 are you performing any gene / sample filtering step?
Your data is very sparse: it's 98% zeroes and more than half of your genes have full zero counts. I don't think DESeq2/ PyDESeq2 can handle this level of sparsity.
I get the issue from the title when running dds.deseq2() after initializing dds as a DeseqDataSet. Any suggestions on how to fix this error?
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