Evidence map›Paper›PMID 21044360›Full record

ArticleBMC bioinformatics2010

Mapping transcription mechanisms from multimodal genomic data.

Hsun-Hsien Chang, Michael McGeachie, Gil Alterovitz, Marco F Ramoni

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Phenotype prediction by integrative network analysis of SNP and gene expression microarrays.Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference · 2011
    Article
  4. Article
  5. Transcriptional network predicts viral set point during acute HIV-1 infection.Journal of the American Medical Informatics Association : JAMIA
    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

4 authors at 3 institutions in 1 country.

Hsun-Hsien ChangChildren's Hospital Informatics Program, Harvard-MIT Division of Health Sciences and Technology, Harvard Medical School, Boston, Massachusetts, USA. hsun-hsien.chang@childrens.harvard.edu
Michael McGeachie
Gil Alterovitz
Marco F Ramoni
Massachusetts Institute of Technology · USBrigham and Women's Hospital · USHarvard–MIT Division of Health Sciences and Technology · US

Funding

Viral Sequencing CoreU19AI067854 · NIAID · DUKE UNIVERSITY · PI CRUMP, JOHN ANDREW · 2006 to 2011
$290.5M
SYSTEMS APPROACHES TO THE EPIDEMIOLOGY, GENETICS AND GENOMICS OF LUNG DISEASEST32HL007427 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI DAWN L DEMEO, Edwin K Silverman · 1985 to 2026
$13.6M
Decoding Gene Expression Control Using Conditional Clustering by DynamicsR01HG003354 · NHGRI · BOSTON CHILDREN'S HOSPITAL · PI RAMONI, MARCO F · 2006 to 2008
$929k
A Holistic Approach to Information Processing for Biomedical NetworksR00LM009826 · NLM · BOSTON CHILDREN'S HOSPITAL · PI ALTEROVITZ, GIL · 2010 to 2012
$727k
A Holistic Approach to Information Processing for Biomedical NetworksK99LM009826 · NLM · BOSTON CHILDREN'S HOSPITAL · PI ALTEROVITZ, GIL · 2008 to 2009
$263k
NHGRI NIH HHS R01HG003354NHLBI NIH HHS T32 HL007427-28NIAID NIH HHS U19 AI067854-05NLM NIH HHS K99 LM009826NLM NIH HHS R00 LM009826
6 · The paper itself

Abstract

backgroundIdentification of expression quantitative trait loci (eQTLs) is an emerging area in genomic study. The task requires an integrated analysis of genome-wide single nucleotide polymorphism (SNP) data and gene expression data, raising a new computational challenge due to the tremendous size of data.

resultsWe develop a method to identify eQTLs. The method represents eQTLs as information flux between genetic variants and transcripts. We use information theory to simultaneously interrogate SNP and gene expression data, resulting in a Transcriptional Information Map (TIM) which captures the network of transcriptional information that links genetic variations, gene expression and regulatory mechanisms. These maps are able to identify both cis- and trans- regulating eQTLs. The application on a dataset of leukemia patients identifies eQTLs in the regions of the GART, PCP4, DSCAM, and RIPK4 genes that regulate ADAMTS1, a known leukemia correlate.

conclusionsThe information theory approach presented in this paper is able to infer the dependence networks between SNPs and transcripts, which in turn can identify cis- and trans-eQTLs. The application of our method to the leukemia study explains how genetic variants and gene expression are linked to leukemia.

Indexed as

GenomeComputational BiologyGene ExpressionGene Expression ProfilingGenetic VariationHumansLeukemiaPolymorphism, Single NucleotideQuantitative Trait LociTranscription, Genetic

Identifiers

PMID21044360
PMCPMC2967743
OpenAlexW2114040365

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.