ArticleThe annals of applied statistics2012
THE SCREENING AND RANKING ALGORITHM TO DETECT DNA COPY NUMBER VARIATIONS.
Article in The annals of applied statistics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.
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Who cites it
29 citing papers in PubMed.
- Computational strategies for copy number variation detection, disease association, and beyond.Genome biology · 2026Review
- Estimation of common breaks in linear panel data models via screening and ranking algorithm.Scientific reports · 2025Article
- Bootstrap-based inference for multiple variance changepoint models.Journal of applied statistics · 2025Article
- Objective Bayesian trend filtering via adaptive piecewise polynomial regression.Journal of applied statistics · 2025Article
- Mobocertinib in Patients with EGFR Exon 20 Insertion-Positive Non-Small Cell Lung Cancer (MOON): An International Real-World Safety and Efficacy Analysis.International journal of molecular sciences · 2024Article
- OTSUCNV: an adaptive segmentation and OTSU-based anomaly classification method for CNV detection using NGS data.BMC genomics · 2024Article
- A Selective Review on Information Criteria in Multiple Change Point Detection.Entropy (Basel, Switzerland) · 2024Review
- Causal Responsibility Division of Chronological Continuous Treatment Based on Change-Point Detection.Entropy (Basel, Switzerland) · 2023Article
- Genetic and methylation profiles distinguish benign, malignant and spitzoid melanocytic tumors.International journal of cancer · 2022Article
- Testing for a Change in Mean After Changepoint Detection.Journal of the Royal Statistical Society. Series B, Statistical methodology · 2022Article
- Genetic and Methylation Analysis of CTNNB1 in Benign and Malignant Melanocytic Lesions.Cancers · 2022Article
- Progress in Methods for Copy Number Variation Profiling.International journal of molecular sciences · 2022Review
- Divergence-Based Segmentation Algorithm for Heavy-Tailed Acoustic Signals with Time-Varying Characteristics.Sensors (Basel, Switzerland) · 2021Article
- Shall genomic correlation structure be considered in copy number variants detection?Briefings in bioinformatics · 2021Article
- A super scalable algorithm for short segment detection.Statistics in biosciences · 2021Article
- Multiple change point detection and validation in autoregressive time series data.Statistical papers (Berlin, Germany) · 2020Article
- CONSISTENT SELECTION OF THE NUMBER OF CHANGE-POINTS VIA SAMPLE-SPLITTING.Annals of statistics · 2020Article
- An accurate and powerful method for copy number variation detection.Bioinformatics (Oxford, England) · 2019Article
- iSeg: an efficient algorithm for segmentation of genomic and epigenomic data.BMC bioinformatics · 2018Article
- modSaRa: a computationally efficient R package for CNV identification.Bioinformatics (Oxford, England) · 2017Article
Corrections and comments
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2 authors.
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Abstract
DNA Copy number variation (CNV) has recently gained considerable interest as a source of genetic variation that likely influences phenotypic differences. Many statistical and computational methods have been proposed and applied to detect CNVs based on data that generated by genome analysis platforms. However, most algorithms are computationally intensive with complexity at least
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