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Klaus F. X. Mayer

dblp:38/4665 · DBLP profile ↗
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8ranked-venue papers
1as first author
0since 2021 · last 2014
0000-0001-6484-1077ORCID · verified

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

Applied, interdisciplinary, general and emerging computing · 8 · 1 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
4 papers
Bioinformatics and computational biology · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gene expression analysis
0.212014
RNASeqExpressionBrowser - a web interface to browse and visualize high-throughput expression data · Bioinform. 2014
Bioinformatics and computational biology › genomics
plant genomics
0.112006
Significant sequence similarities in promoters and precursors of Arabidopsis thaliana non-conserved microRNAs · Bioinform. 2006
Bioinformatics and computational biology › sequence analysis › motif discovery
conserved motif identification
0.112005
CREDO: a web-based tool for computational detection of conserved sequence motifs in noncoding sequences · Bioinform. 2005
Bioinformatics and computational biology › gene regulation
regulatory genomics
0.112005
CREDO: a web-based tool for computational detection of conserved sequence motifs in noncoding sequences · Bioinform. 2005
Bioinformatics and computational biology › genome annotation › gene prediction
comparative gene finding
0.012002
Exon discovery by genomic sequence alignment · Bioinform. 2002
Bioinformatics and computational biology › sequence alignment
genomic sequence alignment
0.012002
Exon discovery by genomic sequence alignment · Bioinform. 2002
Bioinformatics and computational biology
sequence alignment
0.012002
Exon discovery by genomic sequence alignment · Bioinform. 2002
Bioinformatics and computational biology › genome annotation
gene prediction
0.012002
Exon discovery by genomic sequence alignment · Bioinform. 2002

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

web interface · 0.2sequence similarity analysis · 0.1motif discovery algorithms · 0.1local sequence similarity · 0.0cross-species comparison · 0.0
YearPublicationVenuePosition
2014 RNASeqExpressionBrowser - a web interface to browse and visualize high-throughput expression data
abstract
MOTIVATION: RNA-seq techniques generate massive amounts of expression data. Several pipelines (e.g. Tophat and Cufflinks) are broadly applied to analyse these datasets. However, accessing and handling the analytical output remain challenging for non-experts. RESULTS: We present the RNASeqExpressionBrowser, an open-source web interface that can be used to access the output from RNA-seq expression analysis packages in different ways, as it allows browsing for genes by identifiers, annotations or sequence similarity. Gene expression information can be loaded as long as it is represented in a matrix-like format. Additionally, data can be made available by setting up the tool on a public server. For demonstration purposes, we have set up a version providing expression information from the barley genome. AVAILABILITY AND IMPLEMENTATION: The source code and a show case are accessible at http://mips.helmholtz-muenchen.de/plant/RNASeqExpressionBrowser/.
Thomas Nussbaumer, Karl G. Kugler, Kai Christian Bader, Sapna Sharma, Michael Seidel, Klaus F. X. Mayer
Bioinform.6
2007 Apollo2Go: a web service adapter for the Apollo genome viewer to enable distributed genome annotation
abstract
BACKGROUND: Apollo, a genome annotation viewer and editor, has become a widely used genome annotation and visualization tool for distributed genome annotation projects. When using Apollo for annotation, database updates are carried out by uploading intermediate annotation files into the respective database. This non-direct database upload is laborious and evokes problems of data synchronicity. RESULTS: To overcome these limitations we extended the Apollo data adapter with a generic, configurable web service client that is able to retrieve annotation data in a GAME-XML-formatted string and pass it on to Apollo's internal input routine. CONCLUSION: This Apollo web service adapter, Apollo2Go, simplifies the data exchange in distributed projects and aims to render the annotation process more comfortable. The Apollo2Go software is freely available from ftp://ftpmips.gsf.de/plants/apollo_webservice.
Kathrin Klee, Rebecca Ernst, Manuel Spannagl, Klaus F. X. Mayer
BMC Bioinform.4
2006 Significant sequence similarities in promoters and precursors of Arabidopsis thaliana non-conserved microRNAs
abstract
Some plant microRNAs have been shown to be de novo generated by inverted duplication from their target genes. Subsequent duplication events potentially generate multigene microRNA families. Within this article we provide supportive evidence for the inverted duplication model of plant microRNA evolution. First, we report that the precursors of four Arabidopsis thaliana microRNA families, miR157, miR158, miR405 and miR447 share nearly identical nucleotide sequences throughout the whole miRNA precursor between the family members. The extent and degree of sequence conservation is suggestive of recent evolutionary duplication events. Furthermore we found that sequence similarities are not restricted to the transcribed part but extend into the promoter regions. Thus the duplication event most probably included the promoter regions as well. Conserved elements in upstream regions of miR163 and its targets were also detected. This implies that the inverted duplication of target genes, at least in certain cases, had included the promoters of the target genes. Sequence conservation within promoters of miRNA families as well as between miRNA and its potential progenitor gene can be exploited for understanding the regulation of microRNA genes.
Yu Wang 0008, Tobias Hindemitt, Klaus F. X. Mayer
Bioinform.3
2006 Spatiotemporal Expression Control Correlates with Intragenic Scaffold Matrix Attachment Regions (S/MARs) in Arabidopsis thaliana
abstract
Scaffold/matrix attachment regions (S/MARs) are essential for structural organization of the chromatin within the nucleus and serve as anchors of chromatin loop domains. A significant fraction of genes in Arabidopsis thaliana contains intragenic S/MAR elements and a significant correlation of S/MAR presence and overall expression strength has been demonstrated. In this study, we undertook a genome scale analysis of expression level and spatiotemporal expression differences in correlation with the presence or absence of genic S/MAR elements. We demonstrate that genes containing intragenic S/MARs are prone to pronounced spatiotemporal expression regulation. This characteristic is found to be even more pronounced for transcription factor genes. Our observations illustrate the importance of S/MARs in transcriptional regulation and the role of chromatin structural characteristics for gene regulation. Our findings open new perspectives for the understanding of tissue- and organ-specific regulation of gene expression.
Igor V. Tetko, Georg Haberer, Stephen Rudd, Blake C. Meyers, Hans-Werner Mewes, Klaus F. X. Mayer
PLoS Comput. Biol.6
2006 Correction: Spatiotemporal Expression Control Correlates with Intragenic Scaffold Matrix Attachment Regions (S/MARs) in Arabidopsis thaliana
Igor V. Tetko, Georg Haberer, Stephen Rudd, Blake C. Meyers, Hans-Werner Mewes, Klaus F. X. Mayer
PLoS Comput. Biol.6
2005 CREDO: a web-based tool for computational detection of conserved sequence motifs in noncoding sequences
abstract
Abstract Summary: CREDO is a user-friendly, web-based tool that integrates the analysis and results of different algorithms widely used for the computational detection of conserved sequence motifs in noncoding sequences. It enables easy comparison of the individual results. CREDO offers intuitive interfaces for easy and rapid configuration of the applied algorithms and convenient views on the results in graphical and tabular formats. Availability: Contact: [email protected] Supplementary information: A detailed help file for CREDO is available on . Further supplementary material is available on Bioinformatics online.
Tobias Hindemitt, Klaus F. X. Mayer
Bioinform.2
2002 Exon discovery by genomic sequence alignment
abstract
MOTIVATION: During evolution, functional regions in genomic sequences tend to be more highly conserved than randomly mutating 'junk DNA' so local sequence similarity often indicates biological functionality. This fact can be used to identify functional elements in large eukaryotic DNA sequences by cross-species sequence comparison. In recent years, several gene-prediction methods have been proposed that work by comparing anonymous genomic sequences, for example from human and mouse. The main advantage of these methods is that they are based on simple and generally applicable measures of (local) sequence similarity; unlike standard gene-finding approaches they do not depend on species-specific training data or on the presence of cognate genes in data bases. As all comparative sequence-analysis methods, the new comparative gene-finding approaches critically rely on the quality of the underlying sequence alignments. RESULTS: Herein, we describe a new implementation of the sequence-alignment program DIALIGN that has been developed for alignment of large genomic sequences. We compare our method to the alignment programs PipMaker, WABA and BLAST and we show that local similarities identified by these programs are highly correlated to protein-coding regions. In our test runs, PipMaker was the most sensitive method while DIALIGN was most specific. AVAILABILITY: The program is downloadable from the DIALIGN home page at http://bibiserv.techfak.uni-bielefeld.de/dialign/.
Burkhard Morgenstern, Oliver Rinner, Saïd Abdeddaïm, Dirk Haase, Klaus F. X. Mayer, Andreas Dress, Hans-Werner Mewes
Bioinform.5
2000 Arabidopsis Genome Analysis As Exemplified By Analysis of Chromosome 4
abstract
During the last decade the small cruciferous plant Arabidopsis thaliana has become a model organism for flowering plants. Sequencing and analysis of the Arabidopsis genome is nearing completion. Beside an overview on methods and strategies for Arabidopsis genome analysis, a summary of the results from the first analysis is presented. This includes an overview on chromosomal organisation and topological features as well as a first comparison with other genomes.
Klaus F. X. Mayer, Kai Lemcke, Christine M. Schüller, Stephen Rudd, Paolo Zaccaria
Briefings Bioinform.1