Evidence map›Paper›PMID 27733115›Full record

ArticleBMC genomics2016

CNARA: reliability assessment for genomic copy number profiles.

Ni Ai, Haoyang Cai, Caius Solovan, Michael Baudis

Abstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

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2citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. The Progenetix oncogenomic resource in 2021.Database : the journal of biological databases and curation · 2021
    Pooled it
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ni AiInstitute of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Winterthurerstrasse 190, Zurich, CH-8057, Switzerland. ni.ai@uzh.ch.
Haoyang CaiCenter of Growth, Metabolism and Aging, Key Laboratory of Bio-Resources and Eco-Environment, College of Life Sciences, Sichuan University, Chengdu, Sichuan, 610064, China.
Caius SolovanDepartment of Dermatology, "Victor Babeş" University of Medicine and Pharmacy, Timisoara, Romania.
Michael BaudisInstitute of Molecular Life Sciences and Swiss Institute of Bioinformatics, University of Zurich, Winterthurerstrasse 190, Zurich, CH-8057, Switzerland. michael.baudis@imls.uzh.ch.ORCID 0000-0002-9903-4248

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDNA copy number profiles from microarray and sequencing experiments sometimes contain wave artefacts which may be introduced during sample preparation and cannot be removed completely by existing preprocessing methods. Besides, large derivative log ratio spread (DLRS) of the probes correlating with poor DNA quality is sometimes observed in genome screening experiments and may lead to unreliable copy number profiles. Depending on the extent of these artefacts and the resulting misidentification of copy number alterations/variations (CNA/CNV), it may be desirable to exclude such samples from analyses or to adapt the downstream data analysis strategy accordingly.

resultsHere, we propose a method to distinguish reliable genomic copy number profiles from those containing heavy wave artefacts and/or large DLRS. We define four features that adequately summarize the copy number profiles for reliability assessment, and train a classifier on a dataset of 1522 copy number profiles from various microarray platforms. The method can be applied to predict the reliability of copy number profiles irrespective of the underlying microarray platform and may be adapted for those sequencing platforms from which copy number estimates could be computed as a piecewise constant signal. Further details can be found at https://github.com/baudisgroup/CNARA .

conclusionsWe have developed a method for the assessment of genomic copy number profiling data, and suggest to apply the method in addition to and after other state-of-the-art noise correction and quality control procedures. CNARA could be instrumental in improving the assessment of data used for genomic data mining experiments and support the reliable functional attribution of copy number aberrations especially in cancer research.

Indexed as

DNA Copy Number VariationsGene DosageAlgorithmsComputational BiologyComputer SimulationGenomicsReproducibility of ResultsWeb BrowserCNACopy number profileReliability assessment

Identifiers

PMID27733115
PMCPMC5062840

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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.