Evidence map›Paper›PMID 34014778›Full record

ArticleJournal of computational biology : a journal of computational molecular cell biology2021

Deep Large-Scale Multitask Learning Network for Gene Expression Inference.

Kamran Ghasedi Dizaji, Wei Chen, Heng Huang

Open access · greenAbstract read
In one paragraph

Article in Journal of computational biology : a journal of computational molecular cell biology, 2021. 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 49% 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, 5 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

3 authors at 1 institution in 1 country.

Kamran Ghasedi DizajiDepartment of Electrical and Computer Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Wei ChenDepartment of Pediatrics, UPMC Children's Hospital of Pittsburgh, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Heng HuangDepartment of Electrical and Computer Engineering, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
University of Pittsburgh · US

Funding

Imaging Genomics Based Brain Disease PredictionR01AG049371 · NIA · UNIVERSITY OF TEXAS ARLINGTON · PI HUANG, HENG · 2015 to 2019
$2.0M
NIA NIH HHS R01 AG049371
6 · The paper itself

Abstract

Gene expression profiling makes it possible to conduct many biological studies in a variety of fields due to its thorough characterization of cellular states under various experimental conditions. Despite recent advances in high-throughput technology, profiling an entire set of genomes is still difficult and expensive. Due to the high correlation between expression patterns of different genes, the aforementioned problem can be solved with a cost-effective approach that collects only a small subset of genes, called landmark genes, representing the entire set of genes, and infer the remaining genes, called target genes, using a computational model. There are several shallow and deep regression models in literature to estimate the expressions of target genes from the landmark genes. However, the shallow mostly have limited capacity in learning the nonlinear and complex gene expression data and are prone to underfitting, and the deep models generally do not take advantage of correlation among target genes in the learning process and suffer from overfitting. Considering the gene expression inference as a multitask learning problem, we propose a new deep multitask learning algorithm to tackle these issues. Our learning framework automatically learns the correlation between target genes and uses this knowledge to improve its generalization. Specifically, we utilize a subnetwork with low-dimensional latent variables to discover the relationships between target genes and enforce a seamless and easy to implement regularization to our deep regression model. Unlike the existing multitask learning methods that can only deal with dozens or hundreds of tasks, our algorithm is able to efficiently learn the relationships between ∼10,000 target genes and, thus, is scalable to a large number of tasks. Our proposed method outperforms the shallow and deep regression models for gene expression inference and alternative multitask learning algorithms on two large-scale datasets regardless of the network architecture.

Indexed as

Gene Regulatory NetworksAlgorithmsComputational BiologyGene Expression ProfilingGene Expression RegulationMachine LearningModels, Geneticdeep regression modelgene expression inferencelandmark genesmultitask learningtarget genes

Identifiers

PMID34014778
PMCPMC8165479
OpenAlexW3016425191

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.