Evidence map›Paper›PMID 38291375›Full record

ArticleBMC genomics2024

OTSUCNV: an adaptive segmentation and OTSU-based anomaly classification method for CNV detection using NGS data.

Kun Xie, Xiaojun Ge, Haque A K Alvi, Kang Liu, Jianfeng Song, Qiang Yu

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
2.8field-weighted citation impact, top 11% of its field
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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 1 institution in 1 country.

Kun XieSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Xiaojun GeSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Haque A K AlviSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Kang LiuSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China.
Jianfeng SongSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China. jfsong@mail.xidian.edu.cn.
Qiang YuSchool of Computer Science and Technology, Xidian University, Xi'an, 710071, China. qyu@mail.xidian.edu.cn.
Xidian University · CN

Funding

Guangxi Key Laboratory of Trusted Software KX202041the Fundamental Research Funds for the Central Universities under grant ZYTS23213the National Natural Science Foundations of China under grant 62002271
6 · The paper itself

Abstract

Copy-number variations (CNVs), which refer to deletions and duplications of chromosomal segments, represent a significant source of variation among individuals, contributing to human evolution and being implicated in various diseases ranging from mental illness and developmental disorders to cancer. Despite the development of several methods for detecting copy number variations based on next-generation sequencing (NGS) data, achieving robust detection performance for CNVs with arbitrary coverage and amplitude remains challenging due to the inherent complexity of sequencing samples. In this paper, we propose an alternative method called OTSUCNV for CNV detection on whole genome sequencing (WGS) data. This method utilizes a newly designed adaptive sequence segmentation algorithm and an OTSU-based CNV prediction algorithm, which does not rely on any distribution assumptions or involve complex outlier factor calculations. As a result, the effective detection of CNVs is achieved with lower computational complexity. The experimental results indicate that the proposed method demonstrates outstanding performance, and hence it may be used as an effective tool for CNV detection.

Indexed as

AlgorithmsDNA Copy Number VariationsHigh-Throughput Nucleotide SequencingHumansSequence Analysis, DNAWhole Genome SequencingAdaptive segmentationAnomaly detectionCopy number variationNext-generation sequencingOTSU

Identifiers

PMID38291375
PMCPMC10826217
OpenAlexW4391357406

What OpenQuestion holds

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LicenceCC BY
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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.