Evidence map›Paper›PMID 20426691›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2010

The power of detecting enriched patterns: an HMM approach.

Zhiyuan Zhai, Shih-Yen Ku, Yihui Luan, Gesine Reinert, Michael S Waterman, Fengzhu Sun

Abstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Alignment-free sequence comparison based on next-generation sequencing reads.Journal of computational biology : a journal of computational molecular cell biology · 2013
    Article
  3. Normal and compound poisson approximations for pattern occurrences in NGS reads.Journal of computational biology : a journal of computational molecular cell biology · 2012
    Article
  4. Alignment-free sequence comparison (II): theoretical power of comparison statistics.Journal of computational biology : a journal of computational molecular cell biology · 2010
    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

6 authors.

Zhiyuan ZhaiSchool of Mathematics, Shandong University, Jinan, Shandong, PR China.
Shih-Yen Ku
Yihui Luan
Gesine Reinert
Michael S Waterman
Fengzhu Sun

Funding

Implications of haplotype structure in the human genomeP50HG002790 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI TAVARE, SIMON · 2003 to 2013
$29.9M
Computational and Statistical Studies for Multiple Molecular NetworksR21AG032743 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI SUN, FENGZHU · 2008 to 2009
$367k
Biotechnology and Biological Sciences Research CouncilNHGRI NIH HHS P50 HG 002790NIA NIH HHS R21AG032743
6 · The paper itself

Abstract

The identification of binding sites of transcription factors (TF) and other regulatory regions, referred to as motifs, located in a set of molecular sequences is of fundamental importance in genomic research. Many computational and experimental approaches have been developed to locate motifs. The set of sequences of interest can be concatenated to form a long sequence of length n. One of the successful approaches for motif discovery is to identify statistically over- or under-represented patterns in this long sequence. A pattern refers to a fixed word W over the alphabet. In the example of interest, W is a word in the set of patterns of the motif. Despite extensive studies on motif discovery, no studies have been carried out on the power of detecting statistically over- or under-represented patterns Here we address the issue of how the known presence of random instances of a known motif affects the power of detecting patterns, such as patterns within the motif. Let N(W)(n) be the number of possibly overlapping occurrences of a pattern W in the sequence that contains instances of a known motif; such a sequence is modeled here by a Hidden Markov Model (HMM). First, efficient computational methods for calculating the mean and variance of N(W)(n) are developed. Second, efficient computational methods for calculating parameters involved in the normal approximation of N(W)(n) for frequent patterns and compound Poisson approximation of N(W)(n) for rare patterns are developed. Third, an easy to use web program is developed to calculate the power of detecting patterns and the program is used to study the power of detection in several interesting biological examples.

Indexed as

Markov ChainsBase CompositionBase SequenceCpG IslandsInternetNumerical Analysis, Computer-AssistedPattern Recognition, AutomatedPoisson DistributionSequence Analysis, DNA

Identifiers

PMID20426691
PMCPMC3203519

What OpenQuestion holds

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Registered trials

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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.