Evidence map›Paper›PMID 29755832›Full record

ArticleProceedings. IEEE International Conference on Bioinformatics and Biomedicine2017

Collaborative Phenotype Inference from Comorbid Substance Use Disorders and Genotypes.

Jin Lu, Jiangwen Sun, Xinyu Wang, Henry R Kranzler, Joel Gelernter, Jinbo Bi

Open access · greenAbstract read
In one paragraph

Article in Proceedings. IEEE International Conference on Bioinformatics and Biomedicine, 2017. 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
0.4field-weighted citation impact, top 26% 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

6 authors at 3 institutions in 1 country.

Jin LuDepartment of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut.
Jiangwen SunDepartment of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut.
Xinyu WangDepartment of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut.
Henry R KranzlerDepartment of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Joel GelernterDepartments of Psychiatry, Genetics, and Neurobiology, Yale University School of Medicine, New Haven, Connecticut.
Jinbo BiDepartment of Computer Science and Engineering, University of Connecticut, Storrs, Connecticut.
University of Connecticut · USUniversity of Pennsylvania · USYale University · US

Funding

Quantitative methods to subtype drug dependence and detect novel genetic variantsR01DA037349 · NIDA · UNIVERSITY OF CONNECTICUT STORRS · PI BI, JINBO · 2015 to 2018
$1.1M
Classifying addictions using machine learning analysis of multidimensional dataK02DA043063 · NIDA · UNIVERSITY OF CONNECTICUT STORRS · PI BI, JINBO · 2017 to 2021
$809k
NIDA NIH HHS K02 DA043063NIDA NIH HHS R01 DA037349
6 · The paper itself

Abstract

Data in large-scale genetic studies of complex human diseases, such as substance use disorders, are often incomplete. Despite great progress in genotype imputation, e.g., the IMPUTE2 method, considerably less progress has been made in inferring phenotypes. We designed a novel approach to integrate individuals' comorbid conditions with their genotype data to infer missing (unreported) diagnostic criteria of a disorder. The premise of our approach derives from correlations among symptoms and the shared biological bases of concurrent disorders such as co-dependence on cocaine and opioids. We describe a matrix completion method to construct a bi-linear model based on the interactions of genotypes and known symptoms of related disorders to infer unknown values of another set of symptoms or phenotypes. An efficient stochastic and parallel algorithm based on the linearized alternating direction method of multipliers was developed to solve the proposed optimization problem. Empirical evaluation of the approach in comparison with other advanced data matrix completion methods via a case study shows that it both significantly improves imputation accuracy and provides greater computational efficiency.

Identifiers

PMID29755832
PMCPMC5947969
OpenAlexW2771997205

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.