Evidence map›Paper›PMID 22551152›Full record

ArticleAlgorithms for molecular biology : AMB2012

Pattern matching through Chaos Game Representation: bridging numerical and discrete data structures for biological sequence analysis.

Susana Vinga, Alexandra M Carvalho, Alexandre P Francisco, Luís Ms Russo, Jonas S Almeida

Abstract read
In one paragraph

Article in Algorithms for molecular biology : AMB, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Article
  3. NAR genomics and bioinformatics · 2021
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Phylogeny reconstruction based on the length distribution ofAlgorithms for molecular biology : AMB · 2017
    Article
  13. Frontiers in plant science · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Sequence analysis by iterated maps, a review.Briefings in bioinformatics · 2014
    Review
  18. Review
  19. A self-updating road map of The Cancer Genome Atlas.Bioinformatics (Oxford, England) · 2013
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Susana VingaInstituto de Engenharia de Sistemas e Computadores: Investigação e Desenvolvimento (INESC-ID), R, Alves Redol 9, 1000-029 Lisboa, Portugal. svinga@kdbio.inesc-id.pt.
Alexandra M Carvalho
Alexandre P Francisco
Luís Ms Russo
Jonas S Almeida

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChaos Game Representation (CGR) is an iterated function that bijectively maps discrete sequences into a continuous domain. As a result, discrete sequences can be object of statistical and topological analyses otherwise reserved to numerical systems. Characteristically, CGR coordinates of substrings sharing an L-long suffix will be located within 2-L distance of each other. In the two decades since its original proposal, CGR has been generalized beyond its original focus on genomic sequences and has been successfully applied to a wide range of problems in bioinformatics. This report explores the possibility that it can be further extended to approach algorithms that rely on discrete, graph-based representations.

resultsThe exploratory analysis described here consisted of selecting foundational string problems and refactoring them using CGR-based algorithms. We found that CGR can take the role of suffix trees and emulate sophisticated string algorithms, efficiently solving exact and approximate string matching problems such as finding all palindromes and tandem repeats, and matching with mismatches. The common feature of these problems is that they use longest common extension (LCE) queries as subtasks of their procedures, which we show to have a constant time solution with CGR. Additionally, we show that CGR can be used as a rolling hash function within the Rabin-Karp algorithm.

conclusionsThe analysis of biological sequences relies on algorithmic foundations facing mounting challenges, both logistic (performance) and analytical (lack of unifying mathematical framework). CGR is found to provide the latter and to promise the former: graph-based data structures for sequence analysis operations are entailed by numerical-based data structures produced by CGR maps, providing a unifying analytical framework for a diversity of pattern matching problems.

Identifiers

PMID22551152
PMCPMC3402988

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.