Documentation
Simply enter the DNA variant you would like to analyse into the variant field,
select one or multiple transcription factors and click on submit. If you do not
know the location but have a wild-type and a variant sequence, you can still enter them.
In this case, ePOSSUM2 cannot display any known transcription binding sites.
There is detailed documentation of ePOSSUM2's output.
We also provide a disease-linked real-life example.
ePOSSUM2 currently only works with human transcription factors.
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