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Katryn J. Stacey

dblp:68/7969 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2010
0000-0002-3992-7802ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1

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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis › sequence comparison
alignment-free sequence comparison
0.112010
A visual framework for sequence analysis using n-grams and spectral rearrangement · Bioinform. 2010
Bioinformatics and computational biology
protein sequence analysis
0.112010
A visual framework for sequence analysis using n-grams and spectral rearrangement · Bioinform. 2010
Bioinformatics and computational biology › sequence analysis
sequence similarity
0.112010
A visual framework for sequence analysis using n-grams and spectral rearrangement · Bioinform. 2010

Methods — techniques the papers use, named apart from their topics

spectral rearrangement · 0.1n-gram analysis · 0.1
YearPublicationVenuePosition
2010 A visual framework for sequence analysis using n-grams and spectral rearrangement
abstract
MOTIVATION: Protein sequences are often composed of regions that have distinct evolutionary histories as a consequence of domain shuffling, recombination or gene conversion. New approaches are required to discover, visualize and analyze these sequence regions and thus enable a better understanding of protein evolution. RESULTS: Here, we have developed an alignment-free and visual approach to analyze sequence relationships. We use the number of shared n-grams between sequences as a measure of sequence similarity and rearrange the resulting affinity matrix applying a spectral technique. Heat maps of the affinity matrix are employed to identify and visualize clusters of related sequences or outliers, while n-gram-based dot plots and conservation profiles allow detailed analysis of similarities among selected sequences. Using this approach, we have identified signatures of domain shuffling in an otherwise poorly characterized family, and homology clusters in another. We conclude that this approach may be generally useful as a framework to analyze related, but highly divergent protein sequences. It is particularly useful as a fast method to study sequence relationships prior to much more time-consuming multiple sequence alignment and phylogenetic analysis. AVAILABILITY: A software implementation (MOSAIC) of the framework described here can be downloaded from http://bioinformatics.org.au/mosaic/ CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Stefan Maetschke, Karin S. Kassahn, Jasmyn A. Dunn, Siew-Ping Han, Eva Z. Curley, Katryn J. Stacey, Mark A. Ragan
Bioinform.6