Demo Data from EDBT 2026 / reviewers in the wild / expert
Michael A. Quail
dblp:72/7234
· DBLP profile ↗
2ranked-venue papers
0as first author
0since 2021 · last 2016
0000-0002-3861-0483ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2
Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology
functional genomics |
0.2 | 1 | 2016 | The TraDIS toolkit: sequencing and analysis for dense transposon mutant libraries · Bioinform. 2016 |
Bioinformatics and computational biology › functional genomics
transposon insertion sequencing analysis |
0.2 | 1 | 2016 | The TraDIS toolkit: sequencing and analysis for dense transposon mutant libraries · Bioinform. 2016 |
Bioinformatics and computational biology
sequence analysis |
0.1 | 1 | 2016 | The TraDIS toolkit: sequencing and analysis for dense transposon mutant libraries · Bioinform. 2016 |
Bioinformatics and computational biology › sequence analysis › sequencing data analysis
sequencing data analysis pipeline |
0.1 | 1 | 2016 | The TraDIS toolkit: sequencing and analysis for dense transposon mutant libraries · Bioinform. 2016 |
Methods — techniques the papers use, named apart from their topics
illumina sequencing · 0.2PCR amplification · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2016 | The TraDIS toolkit: sequencing and analysis for dense transposon mutant librariesabstractUNLABELLED: Transposon insertion sequencing is a high-throughput technique for assaying large libraries of otherwise isogenic transposon mutants providing insight into gene essentiality, gene function and genetic interactions. We previously developed the Transposon Directed Insertion Sequencing (TraDIS) protocol for this purpose, which utilizes shearing of genomic DNA followed by specific PCR amplification of transposon-containing fragments and Illumina sequencing. Here we describe an optimized high-yield library preparation and sequencing protocol for TraDIS experiments and a novel software pipeline for analysis of the resulting data. The Bio-Tradis analysis pipeline is implemented as an extensible Perl library which can either be used as is, or as a basis for the development of more advanced analysis tools. This article can serve as a general reference for the application of the TraDIS methodology. AVAILABILITY AND IMPLEMENTATION: The optimized sequencing protocol is included as supplementary information. The Bio-Tradis analysis pipeline is available under a GPL license at https://github.com/sanger-pathogens/Bio-Tradis CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online. Lars Barquist, Matthew Mayho, Carla A. Cummins, Amy K. Cain, Christine J. Boinett, Andrew J. Page, Gemma C. Langridge, Michael A. Quail, Jacqueline A. Keane, Julian Parkhill |
Bioinform. | 8 |
| 2009 | The Mycoplasma conjunctivae genome sequencing, annotation and analysisabstractBACKGROUND: The mollicute Mycoplasma conjunctivae is the etiological agent leading to infectious keratoconjunctivitis (IKC) in domestic sheep and wild caprinae. Although this pathogen is relatively benign for domestic animals treated by antibiotics, it can lead wild animals to blindness and death. This is a major cause of death in the protected species in the Alps (e.g., Capra ibex, Rupicapra rupicapra). METHODS: The genome was sequenced using a combined technique of GS-FLX (454) and Sanger sequencing, and annotated by an automatic pipeline that we designed using several tools interconnected via PERL scripts. The resulting annotations are stored in a MySQL database. RESULTS: The annotated sequence is deposited in the EMBL database (FM864216) and uploaded into the mollicutes database MolliGen http://cbi.labri.fr/outils/molligen/ allowing for comparative genomics. CONCLUSION: We show that our automatic pipeline allows for annotating a complete mycoplasma genome and present several examples of analysis in search for biological targets (e.g., pathogenic proteins). Sandra P. Calderon-Copete, George Wigger, Christof Wunderlin, Tobias Schmidheini, Joachim Frey, Michael A. Quail, Laurent Falquet |
BMC Bioinform. | 6 |