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Mitchell J. Sullivan

dblp:39/9391 · DBLP profile ↗
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2ranked-venue papers
2as first author
0since 2021 · last 2016
0000-0001-9076-6963ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author

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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 8 heaviest of 9, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › biological data visualization
haplotype visualization
0.212016
HapFlow: visualizing haplotypes in sequencing data · Bioinform. 2016
Bioinformatics and computational biology › sequence analysis
sequencing data analysis
0.212016
HapFlow: visualizing haplotypes in sequencing data · Bioinform. 2016
Bioinformatics and computational biology
genomics
0.222016
Easyfig: a genome comparison visualizer · Bioinform. 2011
HapFlow: visualizing haplotypes in sequencing data · Bioinform. 2016
Bioinformatics and computational biology › comparative genomics
genome comparison
0.112011
Easyfig: a genome comparison visualizer · Bioinform. 2011
Bioinformatics and computational biology › genomics
genome visualization
0.112011
Easyfig: a genome comparison visualizer · Bioinform. 2011
Bioinformatics and computational biology › genomics
variant analysis
0.112016
HapFlow: visualizing haplotypes in sequencing data · Bioinform. 2016
Bioinformatics and computational biology › sequence alignment › heuristic alignment
BLAST
0.012011
Easyfig: a genome comparison visualizer · Bioinform. 2011
Bioinformatics and computational biology › sequence analysis
sequence comparison
0.012011
Easyfig: a genome comparison visualizer · Bioinform. 2011
YearPublicationVenuePosition
2016 HapFlow: visualizing haplotypes in sequencing data
abstract
SUMMARY: HapFlow is a python application for visualizing haplotypes present in sequencing data. It identifies variant profiles present and reads and creates an abstract visual representation of these profiles to make haplotypes easier to identify. AVAILABILITY AND IMPLEMENTATION: HapFlow is freely available (under a GPL license) for download (for Mac OS X, Unix and Microsoft Windows) from github (http://mjsull.github.io/HapFlow). CONTACT: [email protected].
Mitchell J. Sullivan, Nathan L. Bachmann, Peter Timms, Adam Polkinghorne
Bioinform.1
2011 Easyfig: a genome comparison visualizer
abstract
UNLABELLED: Easyfig is a Python application for creating linear comparison figures of multiple genomic loci with an easy-to-use graphical user interface. BLAST comparisons between multiple genomic regions, ranging from single genes to whole prokaryote chromosomes, can be generated, visualized and interactively coloured, enabling a rapid transition between analysis and the preparation of publication quality figures. AVAILABILITY: Easyfig is freely available (under a GPL license) for download (for Mac OS X, Unix and Microsoft Windows) from the SourceForge web site: http://easyfig.sourceforge.net/.
Mitchell J. Sullivan, Nicola K. Petty, Scott A. Beatson
Bioinform.1