
Hi all,
 I have a question regarding CBS. Once I finish CBS computing, I end up with a text file such as:          sample chromosome     start      stop   mean count
      1 NA06991          1     61736 106013377 -0.002 65870
      2 NA06991          1 106019206 106022376 -1.675    1
      3 NA06991          1 106024056 149036525 -0.002 11462
      4 NA06991          1 149040066 149256692 -0.443   141
      5 NA06991          1 149259417 149436843 -0.144    36 Is there a package that can map the original probe ID or gene IDs to segmentation result? I want to end up with a table that has a column for original probe ID, a column for the related CN mean from CBS, a column for chromosome, and a column for chromosome start position. Thanks a lot for the help! Ying  		 	   		  
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