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tools to get the coverage

I have tried to get the coverage of the reads per base. to do so I used samtools bedcov and bedtools genomecov. I got almost different coverages. do you know what the difference is between these 2 tools?

rna-seq

When posting these kind of questions, please provide:

  • the exact command line for every tool
  • an example of the input data
  • an example of the output data

Without these information, we cannot help you at all, as these tools have a plethora of options, not even talking about all the different kinds of data one can feed in.

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