Evidence map›Paper›PMID 29494600›Full record

ArticlePloS one2018

Computational de novo discovery of distinguishing genes for biological processes and cell types in complex tissues.

Lee A Newberg, Xiaowei Chen, Chinnappa D Kodira, Maria I Zavodszky

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
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  5. Review
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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

4 authors.

Lee A NewbergBiosciences, General Electric Global Research Center, Niskayuna, NY, United States of America.
Xiaowei ChenBiosciences, General Electric Global Research Center, Niskayuna, NY, United States of America.
Chinnappa D KodiraBiosciences, General Electric Global Research Center, Niskayuna, NY, United States of America.
Maria I ZavodszkyBiosciences, General Electric Global Research Center, Niskayuna, NY, United States of America.ORCID 0000-0001-7047-6643

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bulk tissue samples examined by gene expression studies are usually heterogeneous. The data gained from these samples display the confounding patterns of mixtures consisting of multiple cell types or similar cell types in various functional states, which hinders the elucidation of the molecular mechanisms underlying complex biological phenomena. A realistic approach to compensate for the limitations of experimentally separating homogenous cell populations from mixed tissues is to computationally identify cell-type specific patterns from bulk, heterogeneous measurements. We designed the CellDistinguisher algorithm to analyze the gene expression data of mixed samples, identifying genes that best distinguish biological processes and cell types. Coupled with a deconvolution algorithm that takes cell type specific gene lists as input, we show that CellDistinguisher performs as well as partial deconvolution algorithms in predicting cell type composition without the need for prior knowledge of cell type signatures. This approach is also better in predicting cell type signatures than the one-step traditional complete deconvolution methods. To illustrate its wide applicability, the algorithm was tested on multiple publicly available data sets. In each case, CellDistinguisher identified genes reflecting biological processes typical for the tissues and development stages of interest and estimated the sample compositions accurately.

Indexed as

AlgorithmsAnimalsB-LymphocytesBrainGene ExpressionGene Expression ProfilingGenomicsHumansLiverLungOligonucleotide Array Sequence AnalysisRatsSequence Analysis, RNAYeasts

Identifiers

PMID29494600
PMCPMC5832224

What OpenQuestion holds

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LicenceCC BY
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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.