Evidence map›Paper›PMID 32282793›Full record

ArticlePLoS computational biology2020

DRAMS: A tool to detect and re-align mixed-up samples for integrative studies of multi-omics data.

Yi Jiang, Gina Giase, Kay Grennan, Annie W Shieh, Yan Xia, Lide Han, Quan Wang, Qiang Wei, Rui Chen, Sihan Liu and 4 more

Abstract read
In one paragraph

Article in PLoS computational biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
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

14 authors.

Yi JiangCenter for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.ORCID 0000-0002-1196-0280
Gina GiaseSchool of Public Health, University of Illinois at Chicago, Chicago, Illinois, United States of America.ORCID 0000-0001-5924-3195
Kay GrennanDepartment of Psychiatry, SUNY Upstate Medical University, Syracuse, New York, United States of America.
Annie W ShiehDepartment of Psychiatry, SUNY Upstate Medical University, Syracuse, New York, United States of America.
Yan XiaCenter for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.ORCID 0000-0001-6432-9911
Lide HanVanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, Tennessee, United States of America.
Quan WangDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, Tennessee, United States of America.
Qiang WeiDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, Tennessee, United States of America.ORCID 0000-0001-9926-1646
Rui ChenDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, Tennessee, United States of America.ORCID 0000-0002-4341-2908
Sihan LiuCenter for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.
Kevin P WhiteInstitute for Genomics and Systems Biology, Department of Human Genetics, University of Chicago, Chicago, Illinois, United States of America.
Chao ChenCenter for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.ORCID 0000-0002-5114-2282
Bingshan LiDepartment of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, Tennessee, United States of America.ORCID 0000-0003-2129-168X
Chunyu LiuCenter for Medical Genetics & Hunan Key Laboratory of Medical Genetics, School of Life Sciences, Central South University, Changsha, Hunan, China.

Funding

Genetic variants affect brain gene expression and risks of psychiatric disordersU01MH103340 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI LIU, CHUNYU, RZHETSKY, ANDREY · 2014 to 2017
$4.3M
1/2 Measuring translational dynamics and the proteome to identify potential brain biomarkers for psychiatric diseaseR01MH110920 · NIMH · UPSTATE MEDICAL UNIVERSITY · PI LIU, CHUNYU · 2016 to 2019
$2.0M
Integrating epigenomic maps to predict regulatory functions of genetic variantsR01ES024988 · NIEHS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LIU, CHUNYU · 2014 to 2015
$625k
NIEHS NIH HHS R01 ES024988NIMH NIH HHS R01 MH110920NIMH NIH HHS U01 MH103340
6 · The paper itself

Abstract

Studies of complex disorders benefit from integrative analyses of multiple omics data. Yet, sample mix-ups frequently occur in multi-omics studies, weakening statistical power and risking false findings. Accurately aligning sample information, genotype, and corresponding omics data is critical for integrative analyses. We developed DRAMS (https://github.com/Yi-Jiang/DRAMS) to Detect and Re-Align Mixed-up Samples to address the sample mix-up problem. It uses a logistic regression model followed by a modified topological sorting algorithm to identify the potential true IDs based on data relationships of multi-omics. According to tests using simulated data, the more types of omics data used or the smaller the proportion of mix-ups, the better that DRAMS performs. Applying DRAMS to real data from the PsychENCODE BrainGVEX project, we detected and corrected 201 (12.5% of total data generated) mix-ups. Of the 21 mix-ups involving errors of racial identity, DRAMS re-assigned all data to the correct racial group in the 1000 Genomes project. In doing so, quantitative trait loci (QTL) (FDR<0.01) increased by an average of 1.62-fold. The use of DRAMS in multi-omics studies will strengthen statistical power of the study and improve quality of the results. Even though very limited studies have multi-omics data in place, we expect such data will increase quickly with the needs of DRAMS.

Indexed as

Polymorphism, Single NucleotideAlgorithmsChromatinComputational BiologyComputer SimulationEthnicityFemaleFrontal LobeGenomeGenomicsGenotypeHumansLogistic ModelsMaleModels, GeneticOligonucleotide Array Sequence AnalysisChromatin

Identifiers

PMID32282793
PMCPMC7179940

What OpenQuestion holds

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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.