Evidence map›Paper›PMID 31287869›Full record

ArticleNucleic acids research2019

WITER: a powerful method for estimation of cancer-driver genes using a weighted iterative regression modelling background mutation counts.

Lin Jiang, Jingjing Zheng, Johnny S H Kwan, Sheng Dai, Cong Li, Mulin Jun Li, Bolan Yu, Ka F To, Pak C Sham, Yonghong Zhu and 1 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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  5. Network analysis of driver genes in human cancers.Frontiers in bioinformatics · 2024
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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

11 authors.

Lin JiangZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Jingjing ZhengZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Johnny S H KwanDepartmelnt of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, New Territories, Hong Kong.
Sheng DaiZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Cong LiZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Mulin Jun LiDepartment of Pharmacology, School of Basic Medical Sciences, Tianjin Key Laboratory of Inflammation Biology, Tianjin Medical University, Tianjin 300070, China.
Bolan YuKey Laboratory for Major Obstetric Diseases of Guangdong Province, The Third Affiliated Hospital of Guangzhou Medical University, Guangzhou 510150, China.
Ka F ToDepartmelnt of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, New Territories, Hong Kong.
Pak C ShamThe Centre for Genomic Sciences, the University of Hong Kong, Pokfulam, Hong Kong.
Yonghong ZhuZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.
Miaoxin LiZhongshan School of Medicine, Sun Yat-sen University, Guangzhou 510080, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic identification of driver mutations and genes in cancer cells are critical for precision medicine. Due to difficulty in modelling distribution of background mutation counts, existing statistical methods are often underpowered to discriminate cancer-driver genes from passenger genes. Here we propose a novel statistical approach, weighted iterative zero-truncated negative-binomial regression (WITER, http://grass.cgs.hku.hk/limx/witer or KGGSeq,http://grass.cgs.hku.hk/limx/kggseq/), to detect cancer-driver genes showing an excess of somatic mutations. By fitting the distribution of background mutation counts properly, this approach works well even in small or moderate samples. Compared to alternative methods, it detected more significant and cancer-consensus genes in most tested cancers. Applying this approach, we estimated 229 driver genes in 26 different types of cancers. In silico validation confirmed 78% of predicted genes as likely known drivers and many other genes as very likely new drivers for corresponding cancers. The technical advances of WITER enable the detection of driver genes in TCGA datasets as small as 30 subjects and rescue of more genes missed by alternative tools in moderate or small samples.

Indexed as

Gene Expression Regulation, NeoplasticOncogenesSoftwareBenchmarkingComputer SimulationGenomicsHumansInternetMutationNeoplasm ProteinsNeoplasmsRegression AnalysisSample SizeNeoplasm Proteins

Identifiers

PMID31287869
PMCPMC6895256

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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.