Evidence map›Paper›PMID 33520459›Full record

ArticlePeerJ2021

Digital Cell Sorter (DCS): a cell type identification, anomaly detection, and Hopfield landscapes toolkit for single-cell transcriptomics.

Sergii Domanskyi, Alex Hakansson, Thomas J Bertus, Giovanni Paternostro, Carlo Piermarocchi

Abstract read
In one paragraph

Article in PeerJ, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

5 authors.

Sergii DomanskyiDepartment of Physics and Astronomy, Michigan State University, East Lansing, MI, USA.
Alex HakanssonSanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Thomas J BertusDepartment of Physics and Astronomy, Michigan State University, East Lansing, MI, USA.
Giovanni PaternostroSanford Burnham Prebys Medical Discovery Institute, La Jolla, CA, USA.
Carlo PiermarocchiDepartment of Physics and Astronomy, Michigan State University, East Lansing, MI, USA.ORCID 0000-0003-2762-8562

Funding

Data-driven models of hematological cell fate decision and differentiationR01GM122085 · NIGMS · MICHIGAN STATE UNIVERSITY · PI PIERMAROCCHI, CARLO · 2016 to 2020
$1.8M
NIGMS NIH HHS R01 GM122085
6 · The paper itself

Abstract

motivationAnalysis of singe cell RNA sequencing (scRNA-seq) typically consists of different steps including quality control, batch correction, clustering, cell identification and characterization, and visualization. The amount of scRNA-seq data is growing extremely fast, and novel algorithmic approaches improving these steps are key to extract more biological information. Here, we introduce: (i) two methods for automatic cell type identification (i.e., without expert curator) based on a voting algorithm and a Hopfield classifier, (ii) a method for cell anomaly quantification based on isolation forest, and (iii) a tool for the visualization of cell phenotypic landscapes based on Hopfield energy-like functions. These new approaches are integrated in a software platform that includes many other state-of-the-art methodologies and provides a self-contained toolkit for scRNA-seq analysis.

resultsWe present a suite of software elements for the analysis of scRNA-seq data. This Python-based open source software, Digital Cell Sorter (DCS), consists in an extensive toolkit of methods for scRNA-seq analysis. We illustrate the capability of the software using data from large datasets of peripheral blood mononuclear cells (PBMC), as well as plasma cells of bone marrow samples from healthy donors and multiple myeloma patients. We test the novel algorithms by evaluating their ability to deconvolve cell mixtures and detect small numbers of anomalous cells in PBMC data. AVAILABILITY: The DCS toolkit is available for download and installation through the Python Package Index (PyPI). The software can be deployed using the Python import function following installation. Source code is also available for download on Zenodo: DOI 10.5281/zenodo.2533377. SUPPLEMENTARY INFORMATION: Supplemental Materials are available at PeerJ online.

Indexed as

Anomaly detectionAutomatic cell type identificationConsensus annotationHopfield classifierHopfield landscapes visualizationSingle cell RNA sequencingTranscriptome analysis software

Identifiers

PMID33520459
PMCPMC7811293

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.