I will be trying to sequence a specific set of functional genes with the 454 GSJunior...Their size, for example, can range from 800-900 bp. I was wondering if using paired-end sequencing would be the approach to get full sequence length for the respective genes? The idea is to load multiple functional genes onto one lane, each with respective MIDs. I was confused since I thought paired-end was mainly for whole genome sequencing? If I were to use paired-end sequencing, how is the primer design different than 16S rRNA amplicon sequencing? Thanks!

Comment