Evidence map›Paper›PMID 27879477›Full record

ArticleIET systems biology2016

Robust group fused lasso for multisample copy number variation detection under uncertainty.

Hossein Sharifi Noghabi, Majid Mohammadi, Yao-Hua Tan

Abstract read
In one paragraph

Article in IET systems biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Hossein Sharifi NoghabiThe Center of Excellence of Soft Computing and Intelligent Information Processing (SCIIP), Ferdowsi University of Mashhad, Iran. hossein1990@gmail.com.
Majid MohammadiDepartment of Technology, Policy and Management, Delft University of Technology, Netherlands.
Yao-Hua TanDepartment of Technology, Policy and Management, Delft University of Technology, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

One of the most important needs in the post-genome era is providing the researchers with reliable and efficient computational tools to extract and analyse this huge amount of biological data, in which DNA copy number variation (CNV) is a vitally important one. Array-based comparative genomic hybridisation (aCGH) is a common approach in order to detect CNVs. Most of methods for this purpose were proposed for one-dimensional profiles. However, slightly this focus has moved from one- to multi-dimensional signals. In addition, since contamination of these profiles with noise is always an issue, it is highly important to have a robust method for analysing multi-sample aCGH profiles. In this study, the authors propose robust group fused lasso which utilises the robust group total variations. Instead of

Indexed as

Comparative Genomic HybridizationDNA Copy Number VariationsAlgorithmsBreast NeoplasmsComputational BiologyDatabases, GeneticFemaleGenome, HumanHumansModels, StatisticalNormal DistributionPolymorphism, Single NucleotideROC CurveSignal-To-Noise RatioSoftwareUncertainty

Identifiers

PMID27879477
PMCPMC8687376

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.