4.7 Article

The power of word-frequency-based alignment-free functions: a comprehensive large-scale experimental analysis

期刊

BIOINFORMATICS
卷 38, 期 4, 页码 925-932

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btab747

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资金

  1. INdAM -GNCS Project 2019 'Innovative methods for the solution of medical and biological big data'
  2. MIUR-PRIN project 'Multicriteria Data Structures and Algorithms: from compressed to learned indexes, and beyond' [2017WR7SHH]
  3. Universita di Roma-La Sapienza Research Project 2020 'Algoritmi su grafi, limitazioni nel sequenziale e opportunita' nel distribuito'
  4. Italian Association of Cancer Research (AIRC) [IG21837]

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The study focused on a representative set of word-frequency-based AF functions, providing a comprehensive evaluation of their power and Type I error. Results offered novel and informative characterizations of these AF functions, aiding in the selection of functions suitable for analysis tasks.
Motivation: Alignment-free (AF) distance/similarity functions are a key tool for sequence analysis. Experimental studies on real datasets abound and, to some extent, there are also studies regarding their control of false positive rate (Type I error). However, assessment of their power, i.e. their ability to identify true similarity, has been limited to some members of the D-2 family. The corresponding experimental studies have concentrated on short sequences, a scenario no longer adequate for current applications, where sequence lengths may vary considerably. Such a State of the Art is methodologically problematic, since information regarding a key feature such as power is either missing or limited. Results: By concentrating on a representative set of word-frequency-based AF functions, we perform the first coherent and uniform evaluation of the power, involving also Type I error for completeness. Two alternative models of important genomic features (CIS Regulatory Modules and Horizontal Gene Transfer), a wide range of sequence lengths from a few thousand to millions, and different values of k have been used. As a result, we provide a characterization of those AF functions that is novel and informative. Indeed, we identify weak and strong points of each function considered, which may be used as a guide to choose one for analysis tasks. Remarkably, of the 15 functions that we have considered, only four stand out, with small differences between small and short sequence length scenarios. Finally, to encourage the use of our methodology for validation of future AF functions, the Big Data platform supporting it is public.

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