Evidence map›Paper›PMID 31874603›Full record

ArticleBMC bioinformatics2019

A systematic evaluation of copy number alterations detection methods on real SNP array and deep sequencing data.

Fei Luo

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Frontiers in genetics · 2025
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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

1 author at 1 institution in 1 country.

Fei LuoSchool of Computer Science, Wuhan University, Wuhan, China. luofei@whu.edu.cn.
Wuhan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe Copy Number Alterations (CNAs) are discovered to be tightly associated with cancers, so accurately detecting them is one of the most important tasks in the cancer genomics. A series of CNAs detection methods have been proposed and new ones are still being developed. Due to the complexity of CNAs in cancers, no CNAs detection method has been accepted as the gold standard caller. Several evaluation works have made attempts to reveal typical CNAs detection methods' performance. Limited by the scale of evaluation data, these different comparison works don't reach a consensus and the researchers are still confused on how to choose one proper CNAs caller for their analysis. Therefore, it needs a more comprehensive evaluation of typical CNAs detection methods' performance.

resultsIn this work, we use a large-scale real dataset from CAGEKID consortium to evaluate total 12 typical CNAs detection methods. These methods are most widely used in cancer researches and always used as benchmark for the newly proposed CNAs detection methods. This large-scale dataset comprises of SNP array data on 94 samples and the whole genome sequencing data on 10 samples. Evaluations are comprehensively implemented in current scenarios of CNAs detection, which include that detect CNAs on SNP array data, on sequencing data with tumor and normal matched samples and on sequencing data with single tumor sample. Three SNP based methods are firstly ranked. Subsequently, the best SNP based method's results are used as benchmark to compare six matched samples based methods and three single tumor sample based methods in terms of the preprocessing, recall rate, Jaccard index and segmentation characteristics.

conclusionsOur survey thoroughly reveals 12 typical methods' superiority and inferiority. We explain why methods show specific characteristics from a methodological standpoint. Finally, we present the guiding principle for choosing one proper CNAs detection method under specific conditions. Some unsolved problems and expectations are also addressed for upcoming CNAs detection methods.

Indexed as

DNA Copy Number VariationsGenomicsHigh-Throughput Nucleotide SequencingHumansNeoplasmsCopy number alterationsDeep sequencingSNP arrayTumor

Identifiers

PMID31874603
PMCPMC6929333
OpenAlexW2997640910

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.