Evidence map›Paper›PMID 29671394›Full record

ArticleBMC bioinformatics2018

Higher-order partial least squares for predicting gene expression levels from chromatin states.

Shiquan Sun, Xifang Sun, Yan Zheng

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

3 authors.

Shiquan SunSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, Shaanxi, People's Republic of China. sqsun@nwpu.edu.cn.
Xifang SunSchool of Science, Xi'an Shiyou University, Xi'an, 710065, Shaanxi, People's Republic of China.
Yan ZhengSchool of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, Shaanxi, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExtensive studies have shown that gene expression levels are strongly affected by chromatin mark combinations via at least two mechanisms, i.e., activation or repression. But their combinatorial patterns are still unclear. To further understand the relationship between histone modifications and gene expression levels, here in this paper, we introduce a purely geometric higher-order representation, tensor (also called multidimensional array), which might borrow more unknown interactions in chromatin states to predicting gene expression levels.

resultsThe prediction models were learned from regions around upstream 10k base pairs and downstream 10k base pairs of the transcriptional start sites (TSSs) on three species (i.e., Human, Rhesus Macaque, and Chimpanzee) with five histone modifications (i.e., H3K4me1, H3K4me3, H3K27ac, H3K27me3, and Pol II). Experimental results demonstrate that the proposed method is more powerful to predicting gene expression levels than several other popular methods. Specifically, our method enable to get more powerful performance on both commonly used criteria, R and RMSE, as high as 1.7% and 11%, respectively.

conclusionsThe overall aim of this work is to show that the higher-order representation is able to include more unknown interaction information between histone modifications across different species.

Indexed as

Gene Expression RegulationAlgorithmsAnimalsCell LineChromatinComputer SimulationHumansLeast-Squares AnalysisMacaca mulattaPan troglodytesTranscription Initiation SiteChromatinChromatin statesGene expression levelsHigher-order partial least squaresHistone modificationTensor decomposition

Identifiers

PMID29671394
PMCPMC5907142

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.