Evidence map›Paper›PMID 31647523›Full record

ArticleBioinformatics (Oxford, England)2020

SINC: a scale-invariant deep-neural-network classifier for bulk and single-cell RNA-seq data.

Chuanqi Wang, Jun Li

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Chuanqi WangDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, IN 46556, USA.
Jun LiDepartment of Applied and Computational Mathematics and Statistics, University of Notre Dame, Notre Dame, IN 46556, USA.

Funding

Statistical analysis of single cell RNA-sequencing data: detecting dropouts and removing the cell-cycle effectR03CA212964 · NCI · UNIVERSITY OF NOTRE DAME · PI LI, JUN · 2017 to 2018
$155k
NCI NIH HHS R03 CA212964
6 · The paper itself

Abstract

motivationScaling by sequencing depth is usually the first step of analysis of bulk or single-cell RNA-seq data, but estimating sequencing depth accurately can be difficult, especially for single-cell data, risking the validity of downstream analysis. It is thus of interest to eliminate the use of sequencing depth and analyze the original count data directly.

resultsWe call an analysis method 'scale-invariant' (SI) if it gives the same result under different estimates of sequencing depth and hence can use the original count data without scaling. For the problem of classifying samples into pre-specified classes, such as normal versus cancerous, we develop a deep-neural-network based SI classifier named scale-invariant deep neural-network classifier (SINC). On nine bulk and single-cell datasets, the classification accuracy of SINC is better than or competitive to the best of eight other classifiers. SINC is easier to use and more reliable on data where proper sequencing depth is hard to determine. AVAILABILITY AND IMPLEMENTATION: This source code of SINC is available at https://www.nd.edu/∼jli9/SINC.zip. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

NeoplasmsRNA-SeqHumansNeural Networks, ComputerSingle-Cell AnalysisSoftware

Identifiers

PMID31647523
PMCPMC7523643

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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.