Literature DB >> 36035127

Rapid and simple analysis of short and long sequencing reads using DuesselporeTM.

Christian Vogeley1, Thach Nguyen1, Selina Woeste1, Jean Krutmann1, Thomas Haarmann-Stemmann1, Andrea Rossi1.   

Abstract

Transcriptome analysis experiments enable researchers to gain extensive insights into the molecular mechanisms underlying cell physiology and disease. Oxford Nanopore Technologies (ONT) has recently been developed as a fast, miniaturized, portable, and cost-effective alternative to next-generation sequencing (NGS). However, RNA-Seq data analysis software that exploits ONT portability and allows scientists to easily analyze ONT data everywhere without bioinformatics expertise is not widely available. We developed DuesselporeTM, an easy-to-follow deep sequencing workflow that runs as a local webserver and allows the analysis of ONT data everywhere without requiring additional bioinformatics tools or internet connection. DuesselporeTM output includes differentially expressed genes and further downstream analyses, such as variance heatmap, disease and gene ontology plots, gene concept network plots, and exports customized pathways for different cellular processes. We validated DuesselporeTM by analyzing the transcriptomic changes induced by PCB126, a dioxin-like PCB, and a potent aryl hydrocarbon receptor (AhR) agonist in human HaCaT keratinocytes, a well-characterized model system. DuesselporeTM was specifically developed to analyze ONT data, but we also implemented NGS data analysis. DuesselporeTM is compatible with Linux, Microsoft, and Mac operating systems and allows convenient, reliable, and cost-effective analysis of ONT and NGS data.
Copyright © 2022 Vogeley, Nguyen, Woeste, Krutmann, Haarmann-Stemmann and Rossi.

Entities:  

Keywords:  NGS data analysis; Oxford Nanopore MinION device; Oxford nanopore sequencing; RNA-seq analyses; next-generation sequencing

Year:  2022        PMID: 36035127      PMCID: PMC9403543          DOI: 10.3389/fgene.2022.931996

Source DB:  PubMed          Journal:  Front Genet        ISSN: 1664-8021            Impact factor:   4.772


  33 in total

1.  The complete genome of an individual by massively parallel DNA sequencing.

Authors:  David A Wheeler; Maithreyan Srinivasan; Michael Egholm; Yufeng Shen; Lei Chen; Amy McGuire; Wen He; Yi-Ju Chen; Vinod Makhijani; G Thomas Roth; Xavier Gomes; Karrie Tartaro; Faheem Niazi; Cynthia L Turcotte; Gerard P Irzyk; James R Lupski; Craig Chinault; Xing-zhi Song; Yue Liu; Ye Yuan; Lynne Nazareth; Xiang Qin; Donna M Muzny; Marcel Margulies; George M Weinstock; Richard A Gibbs; Jonathan M Rothberg
Journal:  Nature       Date:  2008-04-17       Impact factor: 49.962

2.  Minimap2: pairwise alignment for nucleotide sequences.

Authors:  Heng Li
Journal:  Bioinformatics       Date:  2018-09-15       Impact factor: 6.937

3.  From next-generation sequencing to nanopore sequencing technology: paving the way to personalized genomic medicine.

Authors:  Chee-Seng Ku; Dimitrios H Roukos
Journal:  Expert Rev Med Devices       Date:  2013-01       Impact factor: 3.166

4.  Implementation of Amplicon Parallel Sequencing Leads to Improvement of Diagnosis and Therapy of Lung Cancer Patients.

Authors:  Katharina König; Martin Peifer; Jana Fassunke; Michaela A Ihle; Helen Künstlinger; Carina Heydt; Katrin Stamm; Frank Ueckeroth; Claudia Vollbrecht; Marc Bos; Masyar Gardizi; Matthias Scheffler; Lucia Nogova; Frauke Leenders; Kerstin Albus; Lydia Meder; Kerstin Becker; Alexandra Florin; Ursula Rommerscheidt-Fuss; Janine Altmüller; Michael Kloth; Peter Nürnberg; Thomas Henkel; Sven-Ernö Bikár; Martin L Sos; William J Geese; Lewis Strauss; Yon-Dschun Ko; Ulrich Gerigk; Margarete Odenthal; Thomas Zander; Jürgen Wolf; Sabine Merkelbach-Bruse; Reinhard Buettner; Lukas C Heukamp
Journal:  J Thorac Oncol       Date:  2015-07       Impact factor: 15.609

5.  Identification of genome edited cells using CRISPRnano.

Authors:  Thach Nguyen; Haribaskar Ramachandran; Soraia Martins; Jean Krutmann; Andrea Rossi
Journal:  Nucleic Acids Res       Date:  2022-05-30       Impact factor: 19.160

6.  Somatic mutations in cerebral cortical malformations.

Authors:  Saumya S Jamuar; Anh-Thu N Lam; Martin Kircher; Alissa M D'Gama; Jian Wang; Brenda J Barry; Xiaochang Zhang; Robert Sean Hill; Jennifer N Partlow; Aldo Rozzo; Sarah Servattalab; Bhaven K Mehta; Meral Topcu; Dina Amrom; Eva Andermann; Bernard Dan; Elena Parrini; Renzo Guerrini; Ingrid E Scheffer; Samuel F Berkovic; Richard J Leventer; Yiping Shen; Bai Lin Wu; A James Barkovich; Mustafa Sahin; Bernard S Chang; Michael Bamshad; Deborah A Nickerson; Jay Shendure; Annapurna Poduri; Timothy W Yu; Christopher A Walsh
Journal:  N Engl J Med       Date:  2014-08-21       Impact factor: 91.245

7.  Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease.

Authors:  Manuel A Rivas; Mélissa Beaudoin; Agnes Gardet; Christine Stevens; Yashoda Sharma; Clarence K Zhang; Gabrielle Boucher; Stephan Ripke; David Ellinghaus; Noel Burtt; Tim Fennell; Andrew Kirby; Anna Latiano; Philippe Goyette; Todd Green; Jonas Halfvarson; Talin Haritunians; Joshua M Korn; Finny Kuruvilla; Caroline Lagacé; Benjamin Neale; Ken Sin Lo; Phil Schumm; Leif Törkvist; Marla C Dubinsky; Steven R Brant; Mark S Silverberg; Richard H Duerr; David Altshuler; Stacey Gabriel; Guillaume Lettre; Andre Franke; Mauro D'Amato; Dermot P B McGovern; Judy H Cho; John D Rioux; Ramnik J Xavier; Mark J Daly
Journal:  Nat Genet       Date:  2011-10-09       Impact factor: 38.330

8.  Pathview: an R/Bioconductor package for pathway-based data integration and visualization.

Authors:  Weijun Luo; Cory Brouwer
Journal:  Bioinformatics       Date:  2013-06-04       Impact factor: 6.937

9.  Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.

Authors:  Michael I Love; Wolfgang Huber; Simon Anders
Journal:  Genome Biol       Date:  2014       Impact factor: 13.583

10.  HTSeq--a Python framework to work with high-throughput sequencing data.

Authors:  Simon Anders; Paul Theodor Pyl; Wolfgang Huber
Journal:  Bioinformatics       Date:  2014-09-25       Impact factor: 6.937

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.