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Volker Hollich

dblp:28/3732 · DBLP profile ↗
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3ranked-venue papers
2as first author
0since 2021 · last 2007
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 3 · 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%
Computer graphics and multimedia
1 paper
Visualization and visual analytics · 100%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › protein structure analysis
protein domain analysis
0.112007
PfamAlyzer: domain-centric homology search · Bioinform. 2007
Bioinformatics and computational biology › sequence analysis
sequence similarity search
0.112007
PfamAlyzer: domain-centric homology search · Bioinform. 2007
Bioinformatics and computational biology › comparative genomics › orthology analysis
ortholog identification
0.012002
OrthoGUI: graphical presentation of Orthostrapper results · Bioinform. 2002
Bioinformatics and computational biology › comparative genomics
orthology analysis
0.012002
OrthoGUI: graphical presentation of Orthostrapper results · Bioinform. 2002
Bioinformatics and computational biology › biological database
protein domain database
0.012007
PfamAlyzer: domain-centric homology search · Bioinform. 2007
Visualization and visual analytics
biological data visualization
0.012002
OrthoGUI: graphical presentation of Orthostrapper results · Bioinform. 2002

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

graphical user interface · 0.1clustering · 0.1
YearPublicationVenuePosition
2007 PfamAlyzer: domain-centric homology search
abstract
UNLABELLED: PfamAlyzer is a Java applet that enables exploration of Pfam domain architectures using a user-friendly graphical interface. It can search the UniProt protein database for a domain pattern. Domain patterns similar to the query are presented graphically by PfamAlyzer either in a ranked list or pinned to the tree of life. Such domain-centric homology search can assist identification of distant homologs with shared domain architecture. AVAILABILITY: PfamAlyzer has been integrated with the Pfam database and can be accessed at http://pfam.cgb.ki.se/pfamalyzer.
Volker Hollich, Erik L. L. Sonnhammer
Bioinform.1
2005 Scoredist: A simple and robust protein sequence distance estimator
abstract
BACKGROUND: Distance-based methods are popular for reconstructing evolutionary trees thanks to their speed and generality. A number of methods exist for estimating distances from sequence alignments, which often involves some sort of correction for multiple substitutions. The problem is to accurately estimate the number of true substitutions given an observed alignment. So far, the most accurate protein distance estimators have looked for the optimal matrix in a series of transition probability matrices, e.g. the Dayhoff series. The evolutionary distance between two aligned sequences is here estimated as the evolutionary distance of the optimal matrix. The optimal matrix can be found either by an iterative search for the Maximum Likelihood matrix, or by integration to find the Expected Distance. As a consequence, these methods are more complex to implement and computationally heavier than correction-based methods. Another problem is that the result may vary substantially depending on the evolutionary model used for the matrices. An ideal distance estimator should produce consistent and accurate distances independent of the evolutionary model used. RESULTS: We propose a correction-based protein sequence estimator called Scoredist. It uses a logarithmic correction of observed divergence based on the alignment score according to the BLOSUM62 score matrix. We evaluated Scoredist and a number of optimal matrix methods using three evolutionary models for both training and testing Dayhoff, Jones-Taylor-Thornton, and Muller-Vingron, as well as Whelan and Goldman solely for testing. Test alignments with known distances between 0.01 and 2 substitutions per position (1-200 PAM) were simulated using ROSE. Scoredist proved as accurate as the optimal matrix methods, yet substantially more robust. When trained on one model but tested on another one, Scoredist was nearly always more accurate. The Jukes-Cantor and Kimura correction methods were also tested, but were substantially less accurate. CONCLUSION: The Scoredist distance estimator is fast to implement and run, and combines robustness with accuracy. Scoredist has been incorporated into the Belvu alignment viewer, which is available at ftp://ftp.cgb.ki.se/pub/prog/belvu/.
Erik L. L. Sonnhammer, Volker Hollich
BMC Bioinform.2
2002 OrthoGUI: graphical presentation of Orthostrapper results
abstract
SUMMARY: Orthostrapper is a program that calculates orthology support values for pairs of sequences in a multiple alignment (Storm and Sonnhammer, Bioinformatics, 18, 92-99, 2002). Here we present OrthoGUI, a web interface and display tool for Orthostrapper analysis. OrthoGUI visualizes the Orthostrapper output in both tabular and tree representations, and can also apply a clustering algorithm to identify groups of multiple orthologs, which are indicated by colour coding. AVAILABILITY: http://www.cgb.ki.se/OrthoGUI CONTACT: [email protected]
Volker Hollich, Christian E. V. Storm, Erik L. L. Sonnhammer
Bioinform.1