Optimal Insert Size for TruSeq V2 Sequencing
Illumina's TruSeq Sample Preparation Guide contains a table showing how to modify RNA fragmentation time to get different median insert lengths using the divalent cations and heat method in Appendix B. The median length ranges from 140 to 200 bases. Aren't all of these options wasteful if pairedend 150 bases sequencing is done? I think the ideal inset size would be 300 bases in that case, but if 0 minutes is done, the table shows 200 bases as the median size and you can't do less than 0 minutes! Is there an alternative method which doesn't result is mainly reversecomplemented pairs of reads? Our collaborators' sequencing service uses 8 minutes fragmentation and a plot of the insert sizes shows the mode of the distribution is about 120 bases and the median is about 140 bases so, the majority of reads not only are completely reverse complements of each other, but also have much (or all) of the TruSeq adapter at their ends. The reads are each 150 bases long.
