ArticleBMC bioinformatics2015
SW1PerS: Sliding windows and 1-persistence scoring; discovering periodicity in gene expression time series data.
Article in BMC bioinformatics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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.
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.
Who cites it
18 citing papers in PubMed.
- Topology-enhanced machine learning for speech signal processing.Nature communications · 2026Article
- Automated Quantification of Stereotypical Motor Movements in Autism Using Persistent Homology.bioRxiv : the preprint server for biology · 2025Article
- Detecting Rhythmic Gene Expression in Single-cell Transcriptomics.Journal of biological rhythms · 2024Article
- Nonlinear time series analysis of state-wise COVID-19 in Malaysia using wavelet and persistent homology.Scientific reports · 2024Article
- Detecting Rhythmic Gene Expression in Single Cell Transcriptomics.bioRxiv : the preprint server for biology · 2024Article
- Dynamic topological data analysis: a novel fractal dimension-based testing framework with application to brain signals.Frontiers in neuroinformatics · 2024Article
- A topological data analysis-based method for gait signals with an application to the study of multiple sclerosis.PloS one · 2022Article
- A Survey of Topological Machine Learning Methods.Frontiers in artificial intelligence · 2021Review
- Topological Data Analysis ofFrontiers in artificial intelligence · 2021Article
- Evolutionary homology on coupled dynamical systems with applications to protein flexibility analysis.Journal of applied and computational topology · 2020Article
- TimeTrial: An Interactive Application for Optimizing the Design and Analysis of Transcriptomic Time-Series Data in Circadian Biology Research.Journal of biological rhythms · 2020Article
- Persistent Cohomology for Data With Multicomponent Heterogeneous Information.SIAM journal on mathematics of data science · 2020Article
- Universal method for robust detection of circadian state from gene expression.Proceedings of the National Academy of Sciences of the United States of America · 2018Article
- Gene Coexpression Network Comparison via Persistent Homology.International journal of genomics · 2018Article
- Representability of algebraic topology for biomolecules in machine learning based scoring and virtual screening.PLoS computational biology · 2018Article
- Topological methods for genomics: present and future directions.Current opinion in systems biology · 2017Article
- Windowed persistent homology: A topological signal processing algorithm applied to clinical obesity data.PloS one · 2017Article
- A roadmap for the computation of persistent homology.EPJ data science · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundIdentifying periodically expressed genes across different processes (e.g. the cell and metabolic cycles, circadian rhythms, etc) is a central problem in computational biology. Biological time series may contain (multiple) unknown signal shapes of systemic relevance, imperfections like noise, damping, and trending, or limited sampling density. While there exist methods for detecting periodicity, their design biases (e.g. toward a specific signal shape) can limit their applicability in one or more of these situations.
methodsWe present in this paper a novel method, SW1PerS, for quantifying periodicity in time series in a shape-agnostic manner and with resistance to damping. The measurement is performed directly, without presupposing a particular pattern, by evaluating the circularity of a high-dimensional representation of the signal. SW1PerS is compared to other algorithms using synthetic data and performance is quantified under varying noise models, noise levels, sampling densities, and signal shapes. Results on biological data are also analyzed and compared.
resultsOn the task of periodic/not-periodic classification, using synthetic data, SW1PerS outperforms all other algorithms in the low-noise regime. SW1PerS is shown to be the most shape-agnostic of the evaluated methods, and the only one to consistently classify damped signals as highly periodic. On biological data, and for several experiments, the lists of top 10% genes ranked with SW1PerS recover up to 67% of those generated with other popular algorithms. Moreover, the list of genes from data on the Yeast metabolic cycle which are highly-ranked only by SW1PerS, contains evidently non-cosine patterns (e.g. ECM33, CDC9, SAM1,2 and MSH6) with highly periodic expression profiles. In data from the Yeast cell cycle SW1PerS identifies genes not preferred by other algorithms, hence not previously reported as periodic, but found in other experiments such as the universal growth rate response of Slavov. These genes are BOP3, CDC10, YIL108W, YER034W, MLP1, PAC2 and RTT101.
conclusionsIn biological systems with low noise, i.e. where periodic signals with interesting shapes are more likely to occur, SW1PerS can be used as a powerful tool in exploratory analyses. Indeed, by having an initial set of periodic genes with a rich variety of signal types, pattern/shape information can be included in the study of systems and the generation of hypotheses regarding the structure of gene regulatory networks.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.