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Is it possible to include reads pseudo-aligned to multiple genes using kallisto quant for bulk RNAseq data? I have an index of only multi-copy genes and do not want to discard data due to multi-"mapping".
The text was updated successfully, but these errors were encountered:
I don’t understand the question. Kallisto (by virtue of it being an pseudoalignment algorithm) always retains multimapping information and uses it to generate the estimated counts in the abundance output file.
Is it possible to include reads pseudo-aligned to multiple genes using kallisto quant for bulk RNAseq data? I have an index of only multi-copy genes and do not want to discard data due to multi-"mapping".
The text was updated successfully, but these errors were encountered: