Hello,

In preparation to analyse my own ChIP-seq data, I am trying to follow the steps 
described in this sample workflow:

http://www.bioconductor.org/workshops/2008/SeattleNov08/ChIP-seq/workflow.pdf

The document starts by loading data that has been "reduced to a set of 
alignment start positions (including orientation)".

Can somebody elaborate on that a little bit or, ideally, show it with one 
example?

Also, as part of the reduction, the procedure "removed all duplicate reads and 
applied a quality score cutoff". The score cutoff is fine but how is removing 
duplicates justified?

Thank you,

Ivan




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