P0048
Efficiency Genome Assembly with the Hi-Q Enzyme on an Ion Torrent PGM Sequencing Platform

Date: Monday, January 12, 2015
Room:
Artur Luiz Costa Silva , Universidade Federal do Pará, Belém, Brazil
Despite the high accuracy obtained through high throughput sequencing (HTS) platforms, including sequencing methods such as pyrosequencing (Roche 454), ligase (SOLiD System), and recently post-light sequencing using the Ion Torrent PGM (personal genome machine) that is able to detect ions released during sequencing, there are still many errors inherent in the chemistry used by these platforms. Thus, efforts to address these problems have been undertaken by the sequencing companies. To improve the accuracy of the Ion Torrent PGM reads, Life Technologies has developed an enzyme called Hi-Q.

This work aims to demonstrate the performance of the genome assembly of Corynebacterium pseudotuberculosis Cp31 using the enzyme Hi-Q. To evaluate the results, we used an Ion Torrent dataset obtained without the enzyme for the same strain.

The sequencing using the Hi-Q enzyme affected the accuracy of the reads, improving the assembly quality. As a result, a high number of complete genes related to the reference genome were obtained compared to the previous data (without Hi-Q). Furthermore, the use of Hi-Q reduced the number of contigs  (with the same amount of bases) compared to the previous library. After evaluated the GC bias in the genome produced through the Hi-Q, we identified a reduction of GC-Bias, what can reduce the amount and size of gaps generated in the genome assembly process.

Thus, the high efficiency of Hi-Q enzyme was validated, which will be useful to whole-genome sequencing and RNA-Seq projects, due to its high accuracy, compared