Evidence map›Paper›PMID 33230549›Full record

ArticleBriefings in bioinformatics2021

SSMD: a semi-supervised approach for a robust cell type identification and deconvolution of mouse transcriptomics data.

Xiaoyu Lu, Szu-Wei Tu, Wennan Chang, Changlin Wan, Jiashi Wang, Yong Zang, Baskar Ramdas, Reuben Kapur, Xiongbin Lu, Sha Cao and 1 more

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

11 authors.

Xiaoyu LuDepartment of BioHealth Informatics, Indiana University-Purdue University Indianapolis.
Szu-Wei TuDepartment of BioHealth Informatics, Indiana University-Purdue University Indianapolis.
Wennan ChangDepartment of Electrical and Computer Engineering, Purdue University.
Changlin WanDepartment of Electrical and Computer Engineering, Purdue University.
Jiashi WangBiomedical Data Research Data (BDRD) Lab at Indiana University School of Medicine.
Yong ZangDepartment of Biostatistics and a member of the Center for Computational Biology and Bioinformatics, Indiana University School of Medicine.
Baskar RamdasDepartment of Pediatrics, Indiana University School of Medicine.
Reuben KapurDepartment of Pediatrics, Indiana University School of Medicine.
Xiongbin LuDepartment of Medical and Molecular Genetics, Indiana University School of Medicine.
Sha CaoComputational Biology and Bioinformatics, Indiana University School of Medicine.
Chi ZhangCenter for Computational Biology and Bioinformatics, Indiana University School of Medicine.

Funding

Project-005U54DK106846 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Reuben Kapur, Karen Elizabeth Pollok · 2015 to 2026
$9.7M
Role of p21 activated kinase in LeukemogenesisR01CA173852 · NCI · INDIANA UNIVERSITY INDIANAPOLIS · PI KAPUR, REUBEN · 2014 to 2025
$3.4M
Hyperglycemia mediated myeloproliferative diseaseR01HL140961 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI KAPUR, REUBEN · 2019 to 2022
$2.3M
Targeting Novel Pathways in JMMLR01HL146137 · NHLBI · INDIANA UNIVERSITY INDIANAPOLIS · PI KAPUR, REUBEN · 2019 to 2022
$2.2M
Construction of cell specific gene co-regulations signatures based on single cell transcriptomics analysisR01GM131399 · NIGMS · SOUTH DAKOTA STATE UNIVERSITY · PI MA, QIN · 2018 to 2021
$1.3M
NCI NIH HHS R01 CA173852NHLBI NIH HHS R01 HL140961NHLBI NIH HHS R01 HL146137NIDDK NIH HHS U54 DK106846NIGMS NIH HHS R01 GM131399
6 · The paper itself

Abstract

Deconvolution of mouse transcriptomic data is challenged by the fact that mouse models carry various genetic and physiological perturbations, making it questionable to assume fixed cell types and cell type marker genes for different data set scenarios. We developed a Semi-Supervised Mouse data Deconvolution (SSMD) method to study the mouse tissue microenvironment. SSMD is featured by (i) a novel nonparametric method to discover data set-specific cell type signature genes; (ii) a community detection approach for fixing cell types and their marker genes; (iii) a constrained matrix decomposition method to solve cell type relative proportions that is robust to diverse experimental platforms. In summary, SSMD addressed several key challenges in the deconvolution of mouse tissue data, including: (i) varied cell types and marker genes caused by highly divergent genotypic and phenotypic conditions of mouse experiment; (ii) diverse experimental platforms of mouse transcriptomics data; (iii) small sample size and limited training data source and (iv) capable to estimate the proportion of 35 cell types in blood, inflammatory, central nervous or hematopoietic systems. In silico and experimental validation of SSMD demonstrated its high sensitivity and accuracy in identifying (sub) cell types and predicting cell proportions comparing with state-of-the-arts methods. A user-friendly R package and a web server of SSMD are released via https://github.com/xiaoyulu95/SSMD.

Indexed as

Antigens, DifferentiationCellular MicroenvironmentComputational BiologyDatabases, GeneticGene Expression ProfilingTranscriptomeAnimalsMiceOrgan SpecificityAntigens, Differentiationcancer microenvironmentmouse omics datasemi-supervised learningtissue data deconvolution

Identifiers

PMID33230549
PMCPMC8294548

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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.