Evidence map›Paper›PMID 35136070›Full record

ArticleNature communications2022

SMAP is a pipeline for sample matching in proteogenomics.

Ling Li, Mingming Niu, Alyssa Erickson, Jie Luo, Kincaid Rowbotham, Kai Guo, He Huang, Yuxin Li, Yi Jiang, Junguk Hur and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. 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
0.8field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

13 authors at 6 institutions in 2 countries.

Ling LiDepartment of Biology, University of North Dakota, Grand Forks, ND, 58202, USA.ORCID 0000-0001-6295-2128
Mingming NiuDepartments of Structural Biology and Developmental Neurobiology, Center for Proteomics and Metabolomics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0003-3666-4450
Alyssa EricksonDepartment of Biology, University of North Dakota, Grand Forks, ND, 58202, USA.ORCID 0000-0003-4528-314X
Jie LuoState Key Laboratory for Managing Biotic and Chemical Threats to the Quality and Safety of Agro-products, Zhejiang Academy of Agricultural Sciences, Hangzhou, 310021, China.
Kincaid RowbothamDepartment of Biology, University of North Dakota, Grand Forks, ND, 58202, USA.
Kai GuoDepartment of Neurology, University of Michigan, Ann Arbor, MI, 48109, USA.
He HuangDepartment of Biology, University of North Dakota, Grand Forks, ND, 58202, USA.
Yuxin LiDepartments of Structural Biology and Developmental Neurobiology, Center for Proteomics and Metabolomics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-9739-9860
Yi JiangDepartment of Epidemiology and Biostatistics, School of Public Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430030, China.ORCID 0000-0002-1196-0280
Junguk HurDepartment of Biomedical Sciences, School of medicine and health sciences, University of North Dakota, Grand Forks, ND, 58202, USA.ORCID 0000-0002-0736-2149
Chunyu LiuDepartment of Psychiatry, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.
Junmin PengDepartments of Structural Biology and Developmental Neurobiology, Center for Proteomics and Metabolomics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA. junmin.peng@stjude.org.ORCID 0000-0003-0472-7648
Xusheng WangDepartment of Biology, University of North Dakota, Grand Forks, ND, 58202, USA. xusheng.wang@und.edu.ORCID 0000-0002-1759-9588
University of North Dakota · USSt. Jude Children's Research Hospital · USHuazhong University of Science and Technology · CNSUNY Upstate Medical University · USUniversity of Michigan · USZheJiang Academy of Agricultural Sciences · CN

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
The role of class IIa Hdac in regulating cell fate choice in early cortical development.P20GM104360 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI VAUGHAN, ROXANNE A · 2013 to 2023
$21.1M
Tracking and Evaluation CoreU54GM128729 · NIGMS · UNIVERSITY OF NORTH DAKOTA · PI BASSON, MARC D. · 2018 to 2022
$20.3M
2/2-Discovery and validation of neuronal enhancers associated with the development of psychiatric disordersU01MH116489 · NIMH · UNIVERSITY OF CHICAGO · PI GAYNOR, SOPHIA, GESCHWIND, DANIEL H · 2018 to 2022
$4.5M
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
TIM Project NIDA P30 CenterP30DA044223 · NIDA · UNIVERSITY OF TENNESSEE HEALTH SCI CTR · PI SABA, LAURA MAREN, WILLIAMS, ROBERT W. · 2017 to 2021
$3.9M
Multi-level Integrative Proteomics to Alzheimer's Disease PathwaysR01AG053987 · NIA · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI PENG, JUNMIN · 2016 to 2020
$2.2M
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
NCI NIH HHS P30 CA021765NIA NIH HHS R01 AG053987NIDA NIH HHS P30 DA044223NIGMS NIH HHS P20 GM104360NIGMS NIH HHS U54 GM128729NIMH NIH HHS R01 MH110920NIMH NIH HHS U01 MH103340NIMH NIH HHS U01 MH116489
6 · The paper itself

Abstract

The integration of genomics and proteomics data (proteogenomics) holds the promise of furthering the in-depth understanding of human disease. However, sample mix-up is a pervasive problem in proteogenomics because of the complexity of sample processing. Here, we present a pipeline for Sample Matching in Proteogenomics (SMAP) to verify sample identity and ensure data integrity. SMAP infers sample-dependent protein-coding variants from quantitative mass spectrometry (MS), and aligns the MS-based proteomic samples with genomic samples by two discriminant scores. Theoretical analysis with simulated data indicates that SMAP is capable of uniquely matching proteomic and genomic samples when ≥20% genotypes of individual samples are available. When SMAP was applied to a large-scale dataset generated by the PsychENCODE BrainGVEX project, 54 samples (19%) were corrected. The correction was further confirmed by ribosome profiling and chromatin sequencing (ATAC-seq) data from the same set of samples. Our results demonstrate that SMAP is an effective tool for sample verification in a large-scale MS-based proteogenomics study. SMAP is publicly available at https://github.com/UND-Wanglab/SMAP , and a web-based version can be accessed at https://smap.shinyapps.io/smap/ .

Indexed as

Datasets as TopicChromatin Immunoprecipitation SequencingData AnalysisFemaleHumansMaleMass SpectrometryProteogenomicsRNA-SeqSoftwareWhole Genome Sequencing

Identifiers

PMID35136070
PMCPMC8825821
OpenAlexW4210879312

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.