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Old 02-16-2012, 03:47 PM   #3
Location: Alaska

Join Date: Jan 2012
Posts: 49

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????
Anyone remember the days were you just dumped 3 volumes of Maniatis on a student desk and turned around... probably not.
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