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RNA-seq

RNA-seq

RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...

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Updated: Dec 27, 2025

Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq

Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq

Published on: March 12, 2021

Corrigendum: Digitaldlsorter: Deep-Learning on scRNA-Seq to Deconvolute Gene Expression Data.

Carlos Torroja¹, Fatima Sanchez-Cabo¹

¹Bioinformatics Unit, Fundación Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.

Frontiers in Genetics

|March 3, 2020

Summary

This summary is machine-generated.

This study corrects the article DOI for a genetics research paper. The corrected DOI ensures proper citation and access to the published findings in the field of genetics.

Keywords:

cancer deconvolution algorithm immunology machine learning single-cell

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Area of Science:

Genetics research
Molecular biology
Bioinformatics

Context:

Ensuring accurate scientific record-keeping
Facilitating proper citation of research
Maintaining integrity of scientific publications

Purpose:

To provide the correct Digital Object Identifier (DOI) for a published article
To rectify an error in the original publication's metadata
To improve discoverability and citation tracking

Summary:

The article DOI: 10.3389/fgene.2019.00978 has been corrected.
This correction ensures accurate referencing for future research.
The intended article is now correctly identified within the scientific literature.

Impact:

Improved accuracy in scientific literature
Enhanced accessibility to research findings
Facilitation of reliable scientific communication