Unknown

Dataset Information

0

CASPER: context-aware scheme for paired-end reads from high-throughput amplicon sequencing.


ABSTRACT: Merging the forward and reverse reads from paired-end sequencing is a critical task that can significantly improve the performance of downstream tasks, such as genome assembly and mapping, by providing them with virtually elongated reads. However, due to the inherent limitations of most paired-end sequencers, the chance of observing erroneous bases grows rapidly as the end of a read is approached, which becomes a critical hurdle for accurately merging paired-end reads. Although there exist several sophisticated approaches to this problem, their performance in terms of quality of merging often remains unsatisfactory. To address this issue, here we present a context-aware scheme for paired-end reads (CASPER): a computational method to rapidly and robustly merge overlapping paired-end reads. Being particularly well suited to amplicon sequencing applications, CASPER is thoroughly tested with both simulated and real high-throughput amplicon sequencing data. According to our experimental results, CASPER significantly outperforms existing state-of-the art paired-end merging tools in terms of accuracy and robustness. CASPER also exploits the parallelism in the task of paired-end merging and effectively speeds up by multithreading. CASPER is freely available for academic use at http://best.snu.ac.kr/casper.

SUBMITTER: Kwon S 

PROVIDER: S-EPMC4168710 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

altmetric image

Publications

CASPER: context-aware scheme for paired-end reads from high-throughput amplicon sequencing.

Kwon Sunyoung S   Lee Byunghan B   Yoon Sungroh S  

BMC bioinformatics 20140910


Merging the forward and reverse reads from paired-end sequencing is a critical task that can significantly improve the performance of downstream tasks, such as genome assembly and mapping, by providing them with virtually elongated reads. However, due to the inherent limitations of most paired-end sequencers, the chance of observing erroneous bases grows rapidly as the end of a read is approached, which becomes a critical hurdle for accurately merging paired-end reads. Although there exist sever  ...[more]

Similar Datasets

| S-EPMC4582294 | biostudies-literature
| S-EPMC3614465 | biostudies-other
| S-EPMC7168855 | biostudies-literature
| S-EPMC6302405 | biostudies-literature
| S-EPMC5834899 | biostudies-literature
| S-EPMC3076424 | biostudies-literature
| S-EPMC4074385 | biostudies-literature
| S-EPMC6878638 | biostudies-literature
| S-EPMC3018808 | biostudies-other
| S-EPMC3919575 | biostudies-literature