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Old 02-16-2012, 11:25 AM   #2
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Location: Boston area

Join Date: Nov 2007
Posts: 747

Originally Posted by rd69 View Post
I started working on whole genome sequencing and exome sequencing with Illumina HiSeq 2000 and also with 454 sequencer. Can anybody please help me to understand the data analysis of the sequenced reads????
If you'd like answers to such a question, you should start by posting in the correct forum. Then, explain what you want to do with the reads. You're query can be condensed to "I ran an experiment; how do I analyze it?", and nobody can really help you without some real detail.
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