Evidence map›Paper›PMID 22125395›Full record

ArticleBioinformation2011

Classifying DNA repair genes by kernel-based support vector machines.

Hao Jiang, Wai-Ki Ching

Open access · hybridAbstract read
In one paragraph

Article in Bioinformation, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 41% 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, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
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

2 authors at 1 institution in 1 country.

Hao JiangAdvanced Modeling and Applied Computing Laboratory, Department of Mathematics, University of Hong Kong, Pokfulam Road, Hong Kong.
Wai-Ki Ching
University of Hong Kong · HK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human longevity is a complex phenotype that has a significant genetic predisposition. Like other biological processes, ageing process is governed through the regulation of signaling pathways and transcription factors. The DNA damage theory of ageing suggests that ageing is a consequence of un-repaired DNA damage accumulation. Intensive research has been carried out to elucidate the role of DNA repair systems in the ageing process. Decision Trees and Naive Bayesian Algorithm are two data-mining based classification methods for systematically analyzing data about human DNA repair genes. In this paper we develop a linearly combined kernel with Support Vector Machine (SVM) to analyze the ageing related data. The popular supervised learning algorithm enables better discrimination between ageing-related and non-ageing-related DNA repair genes. The linear combination of linear kernel and polynomial kernel of degree 3 in conjunction with SVM allows better classification accuracy in DNA repair gene data set. Compared to Decision Trees and Naive Bayesian Algorithm, SVM with the proposed kernel can achieve 65% AUC (Area Under ROC Curve) values, in contrast to 51.1% and 52.1% respectively. More importantly, we obtain 5 significant ageingrelated genes selected through the training on the whole data set and they are PCNA, PARP, APEX1, MLH1 and XRCC6. Different from the two methods, we can identify another important gene PCNA in the pathways the two methods targeted, while they failed to. And two novel genes PARP, MLH1 are selected as well. The two genes might provide potential insights for biologists in ageing research. SVM is a powerful and robust classification algorithm that can yield higher predictive accuracies. The selection of proper kernel plays a more important role in fulfilling the classification task. The important genes identified not only can target critical pathways related to ageing but also detected genes that may reveal possible related ageing biomarkers.

Identifiers

PMID22125395
PMCPMC3218421
OpenAlexW2064755097

What OpenQuestion holds

Textmetadata
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.