A Long Fragment Aligner called ALFALFA

BMC Bioinformatics. 2015 May 15;16(1):159. doi: 10.1186/s12859-015-0533-0.

Abstract

Background: Rapid evolutions in sequencing technology force read mappers into flexible adaptation to longer reads, changing error models, memory barriers and novel applications.

Results: ALFALFA achieves a high performance in accurately mapping long single-end and paired-end reads to gigabase-scale reference genomes, while remaining competitive for mapping shorter reads. Its seed-and-extend workflow is underpinned by fast retrieval of super-maximal exact matches from an enhanced sparse suffix array, with flexible parameter tuning to balance performance, memory footprint and accuracy.

Conclusions: ALFALFA is open source and available at http://alfalfa.ugent.be .

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms
  • Biological Evolution
  • Genome, Human*
  • High-Throughput Nucleotide Sequencing / methods*
  • Humans
  • Sequence Alignment / methods*
  • Sequence Analysis, DNA / methods*
  • Software*
  • Workflow