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Updated: Aug 5, 2026

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Ultra-long Read Sequencing for Whole Genomic DNA Analysis
Published on: March 15, 2019
NextLongIso: a comprehensive Nextflow pipeline for multi-dimensional long-read RNA-seq analysis
Jiang Tan1,2,3,4, Yuqing Wu2,3,4, Yidan Sun1,2,3,4
1Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, USA.
Bioinformatics (Oxford, England)
|August 3, 2026
Summary
NextLongIso is a new Nextflow pipeline that unifies the analysis of long-read RNA sequencing data. It enables comprehensive characterization of transcript structure, regulation, and variation from PacBio and ONT datasets.
Area of Science:
- Genomics
- Transcriptomics
- Bioinformatics
Background:
- Long-read RNA sequencing (RNA-seq) technologies like PacBio and ONT offer direct full-length transcript characterization.
- Current analysis of long-read RNA-seq data is fragmented across multiple tools, hindering a unified view of transcriptomic complexity.
Purpose of the Study:
- To present NextLongIso, a scalable and reproducible Nextflow pipeline for coordinated analysis of long-read RNA-seq data.
- To integrate transcript discovery with downstream regulatory analyses for a comprehensive understanding of transcriptomic variation.
Main Methods:
- NextLongIso is implemented in Nextflow, ensuring scalability and reproducibility.
- The pipeline integrates transcript discovery with analyses of alternative splicing, isoform switching, transcript boundary dynamics, and transposable element transcription.
- It supports both PacBio and Oxford Nanopore Technologies (ONT) datasets.
Main Results:
- NextLongIso provides a unified framework for analyzing multiple layers of transcript regulation.
- It facilitates joint characterization of alternative splicing, isoform switching, and transcript boundary dynamics.
- The pipeline enables the analysis of transposable element-associated transcription from long-read data.
Conclusions:
- NextLongIso streamlines the analysis of long-read RNA-seq data by eliminating the need for complex cross-tool data harmonization.
- This unified framework facilitates the transition from transcript identification to the functional interpretation of transcriptomic variation.
- It enhances the ability to obtain a comprehensive view of transcript structure, expression, and regulatory variation.
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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 microarray-based...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Next-generation Sequencing
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
