Hi all,
I am new to the field. Here is a silly question:
For quantification of defined genomic regions (let it be genes, windows, etc) based on sequencing data, why do people rarely count base-pairs (a convenient function for doing that is "coverage" in R) but rather count reads?
Thanks in advance,
Yue
I am new to the field. Here is a silly question:
For quantification of defined genomic regions (let it be genes, windows, etc) based on sequencing data, why do people rarely count base-pairs (a convenient function for doing that is "coverage" in R) but rather count reads?
Thanks in advance,
Yue
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