CAGEscan mapping protocol

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Revision as of 14:14, 22 March 2011 by Plessy (talk | contribs) (Why the CAGEscan 3′ reads are trimmed.)
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Input

5' and 3' paired-end fastq files

The 6 first bases of the 3′ reads are trimmed because they derive from to the random part (N6) of the reverse-transcription primer, and therefore may not reflect the RNA sequences accurately, since the reverse-transcriptase tolerates mismatches even on the last two bases. See Mizuno et al., 1999 for example of priming over mismatches.

Output

Mapped paired-end tags in BAM format