---------- Forwarded message ----------
From: wang peter <wng.peter@gmail.com>
Date: Wed, Oct 5, 2011 at 3:44 PM
Subject: how to deal with Fastq file more than 30G
To: bioc-sig-sequencing@r-project.org


IT is too slow to read them in the memory.
who can tell me if i need split them by other program or
call some R function to split them

thx

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