Go to main contents Go to main menus

사용자별 맞춤메뉴

자주찾는 메뉴

추가하기
닫기

Research Articles

contents area

detail content area

HIA: a genome mapper using hybrid index-based sequence alignment
  • Date2018-02-13 13:03
  • Update2018-02-13 13:03
  • CountersignatureDivision of Research Planning
  • Tel043-719-8033
Algorithms for Molecular Biology, 2015, 01, 1─9

HIA: a genome mapper using hybrid index-based sequence alignment

Jongpill Choi, Kiejung Park, Seong Beom Cho, Myungguen Chung

Abstract

    Background
    A number of alignment tools have been developed to align sequencing reads to the human reference genome. The scale of information from next-generation sequencing (NGS) experiments, however, is increasing rapidly. Recent studies based on NGS technology have routinely produces exome or whole-genome seqeuences from several hundreds or thousands of samples. To accomodate the increasing need of analyzing very large NGS data sets, it is necessary to develop faster, more sensitive and accurate mapping tools.
    Results
    HIA uses two indices, a hash talbe index and a suffix array index. The has table performs direct lookup of a q-gram, and the suffix array performs very fast lookup of variable-length strings by exploiting binary search. We observed that combining hash table and suffix array (hybrid index) is much faster than suffix array method for finding a substring in the reference sequence. Here, we defined the matching region (MR) is a longest common substring between a reference and a read. And, we also defined the candidate alignment regions (CARs) as a list of MRs that is close to each other. The hybrid index is used to find candiate alignment regions (CARs) between a reference and a read. We found that aligning only the unmatched regions in the CAR is much faster than aligning the whole CAR. In bencemark analysis, HIA outperformed in mapping speed compared with the other aligners, without significant lost of mapping accurary.
    Conclusions
    Our experiments show that the hybrid of hash table and suffix array is useful in terms of speed for mapping NGS seqeuncing reads to the human reference genome sequence. In conclusion, our tool is appropriate for aligning massive data sets generated by NGS sequencing.


  • ISBN or ISSN: 1748-7188

  • 본 연구는 질병관리본부 연구개발과제(과제번호 2013-NG72001-00) 연구비를 지원받아 수행되었습니다.
  • This research was supported by a fund(code 2013-NG72001-00) by Research of Korea Centers for Disease Control and Prevention.


This public work may be used under the terms of the public interest source + commercial use prohibition + nonrepudiation conditions This public work may be used under the terms of the public interest source + commercial use prohibition + nonrepudiation conditions
TOP