Evidence map›Paper›PMID 26753102›Full record

ArticleQuantitative biology (Beijing, China)2015

Multiple functional linear model for association analysis of RNA-seq with imaging.

Junhai Jiang, Nan Lin, Shicheng Guo, Jinyun Chen, Momiao Xiong

Open access · diamondAbstract read
In one paragraph

Article in Quantitative biology (Beijing, China), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

5 authors at 2 institutions in 2 countries.

Junhai JiangHuman Genetics Center, Division of Biostatistics, The University of Texas School of Public Health, Houston, TX 77030, USA.
Nan LinHuman Genetics Center, Division of Biostatistics, The University of Texas School of Public Health, Houston, TX 77030, USA.
Shicheng GuoHuman Genetics Center, Division of Biostatistics, The University of Texas School of Public Health, Houston, TX 77030, USA; State Key Laboratory of Genetic Engineering and Ministry of Education, Key Laboratory of Contemporary Anthropology, Collaborative Innovation Center for Genetics and Development, School of Life Sciences and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China.
Jinyun ChenDepartment of Epidemiology, Division of OVP, Cancer Prevention and Population Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Momiao XiongHuman Genetics Center, Division of Biostatistics, The University of Texas School of Public Health, Houston, TX 77030, USA.
The University of Texas Health Science Center at Houston · USThe University of Texas MD Anderson Cancer Center · US

Funding

Statistical Methods for Finding Missing HeritabilityR01HL106034 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIONG, MOMIAO · 2011 to 2014
$1.5M
Unified Statistical Methods for Sequence-Based Association StudiesR01GM104411 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIONG, MOMIAO · 2013 to 2016
$1.3M
Understanding the genetic architecture of schizophrenia in Chinese populationR01MH101054 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI CHEN, XIANGNING · 2013 to 2015
$602k
Network Approach to GWA Studies of Rheumatoid Arthritis (RA), Ankylosing SpondyliR01AR057120 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI XIONG, MOMIAO · 2009 to 2010
$554k
NHLBI NIH HHS R01 HL106034NIAMS NIH HHS R01 AR057120NIGMS NIH HHS R01 GM104411NIMH NIH HHS R01 MH101054
6 · The paper itself

Abstract

Emerging integrative analysis of genomic and anatomical imaging data which has not been well developed, provides invaluable information for the holistic discovery of the genomic structure of disease and has the potential to open a new avenue for discovering novel disease susceptibility genes which cannot be identified if they are analyzed separately. A key issue to the success of imaging and genomic data analysis is how to reduce their dimensions. Most previous methods for imaging information extraction and RNA-seq data reduction do not explore imaging spatial information and often ignore gene expression variation at the genomic positional level. To overcome these limitations, we extend functional principle component analysis from one dimension to two dimensions (2DFPCA) for representing imaging data and develop a multiple functional linear model (MFLM) in which functional principal scores of images are taken as multiple quantitative traits and RNA-seq profile across a gene is taken as a function predictor for assessing the association of gene expression with images. The developed method has been applied to image and RNA-seq data of ovarian cancer and kidney renal clear cell carcinoma (KIRC) studies. We identified 24 and 84 genes whose expressions were associated with imaging variations in ovarian cancer and KIRC studies, respectively. Our results showed that many significantly associated genes with images were not differentially expressed, but revealed their morphological and metabolic functions. The results also demonstrated that the peaks of the estimated regression coefficient function in the MFLM often allowed the discovery of splicing sites and multiple isoforms of gene expressions.

Indexed as

functional linear modelfunctional principal component analysisimagingimaging genomicsRNA-seq

Identifiers

PMID26753102
PMCPMC4705549
OpenAlexW1779742924

What OpenQuestion holds

Textmetadata
LicenceTDM
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.