Hello, thank you for developing TIGRESS, that is such an interesting framework.
As linear regression makes assumptions about data normality, do you know if it can be safely used on RNA-Seq counts that are better fit by Poisson or negative binomial distributions? Would it be preferable to log transform the data before running TIGRESS?
Out of curiosity, have you ever tried to replace the lars function in the code by a function fitting sparse generalized linear models such as dglars, to model expression counts as a Poisson distribution for example?
Best regards
Hello, thank you for developing TIGRESS, that is such an interesting framework.
As linear regression makes assumptions about data normality, do you know if it can be safely used on RNA-Seq counts that are better fit by Poisson or negative binomial distributions? Would it be preferable to log transform the data before running TIGRESS?
Out of curiosity, have you ever tried to replace the
larsfunction in the code by a function fitting sparse generalized linear models such as dglars, to model expression counts as a Poisson distribution for example?Best regards