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Klaus Heumann

dblp:59/5121 · DBLP profile ↗
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5ranked-venue papers
2as first author
0since 2021 · last 2001
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 4 · 2 first-authorGraphics, computer vision, multimedia, augmented reality and games · 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
4 papers
Bioinformatics and computational biology · 100%
Computer architecture, parallel and distributed computing, and storage systems
1 paper
Distributed systems · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
genome annotation
0.012001
Functional and structural genomics using PEDANT · Bioinform. 2001
Bioinformatics and computational biology › data integration
biological database integration
0.011998
Comprehensive, comprehensible, distributed and intelligent databases: current status · Bioinform. 1998
Bioinformatics and computational biology › genomics
genome visualization
0.011996
A Top-Down Approach to Whole Genome Visualization · ISMB 1996
Distributed systems
distributed database
0.011994
A new concept of sequence data distribution on wide area networks · Comput. Appl. Biosci. 1994
Bioinformatics and computational biology
sequence analysis
0.012001
Functional and structural genomics using PEDANT · Bioinform. 2001
Bioinformatics and computational biology › biological database
sequence database access
0.011994
A new concept of sequence data distribution on wide area networks · Comput. Appl. Biosci. 1994

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

structural prediction · 0.0automated annotation · 0.0remote procedure call · 0.0
YearPublicationVenuePosition
2001 Functional and structural genomics using PEDANT
abstract
MOTIVATION: Enormous demand for fast and accurate analysis of biological sequences is fuelled by the pace of genome analysis efforts. There is also an acute need in reliable up-to-date genomic databases integrating both functional and structural information. Here we describe the current status of the PEDANT software system for high-throughput analysis of large biological sequence sets and the genome analysis server associated with it. RESULTS: The principal features of PEDANT are: (i) completely automatic processing of data using a wide range of bioinformatics methods, (ii) manual refinement of annotation, (iii) automatic and manual assignment of gene products to a number of functional and structural categories, (iv) extensive hyperlinked protein reports, and (v) advanced DNA and protein viewers. The system is easily extensible and allows to include custom methods, databases, and categories with minimal or no programming effort. PEDANT is actively used as a collaborative environment to support several on-going genome sequencing projects. The main purpose of the PEDANT genome database is to quickly disseminate well-organized information on completely sequenced and unfinished genomes. It currently includes 80 genomic sequences and in many cases serves as the only source of exhaustive information on a given genome. The database also acts as a vehicle for a number of research projects in bioinformatics. Using SQL queries, it is possible to correlate a large variety of pre-computed properties of gene products encoded in complete genomes with each other and compare them with data sets of special scientific interest. In particular, the availability of structural predictions for over 300 000 genomic proteins makes PEDANT the most extensive structural genomics resource available on the web.
Dmitrij Frishman, Kaj Albermann, Jean Hani, Klaus Heumann, Agnes Metanomski, Alfred Zollner, Hans-Werner Mewes
Bioinform.4
1998 Comprehensive, comprehensible, distributed and intelligent databases: current status
abstract
MOTIVATION: It is only a matter of time until a user will see not many but one integrated database of information for molecular biology. Is this true? Is it a good thing? Why will it happen? Where are we now? What developments are fostering and what developments are impeding progress towards this end? SUPPLEMENTARY INFORMATION: A list of WWW resources devoted to database issues in molecular biology is available at http://www.mips.biochem.mpg.de CONTACT: [email protected]
Dmitrij Frishman, Klaus Heumann, Arthur M. Lesk, Hans-Werner Mewes
Bioinform.2
1996 A Top-Down Approach to Whole Genome Visualization
Klaus Heumann, C. Harris, Hans-Werner Mewes
ISMB1
1995 Genome Analysis: Pattern Search in Biological Macromolecules
Hans-Werner Mewes, Klaus Heumann
CPM2
1994 A new concept of sequence data distribution on wide area networks
abstract
Accepted concepts in distributed applications design have been applied in the development of a network-based system for the synchronization of remote sequence database access sites by an incremental update mechanism. Computer hardware requirements, network bandwidth, and stability considerations make centralized access to essential computerized resources undesirable. A network model has been developed to distribute access over a collection of remotely situated computer centers. The formally independent database-access nodes join to form a heterogeneous, long distance, co-operating network that can compensate for the deficiencies of unstable network links thereby ensuring uninterrupted access to the resource. In order to guarantee consistency among these nodes, several distributed transaction protocols have been investigated; based on these results, a prototype system has been implemented. A layered software architecture makes the distributed transaction protocol transparent to the individual database system and the underlying network. Individual components of this network communicate by means of Remote Procedure Calls (RPCs). A prototype software system operates to synchronize up to data copies of the PIR-International Protein Sequence Database (Barker et al., 1993) at a number of different sites using the public Internet as the transport vehicle.
Klaus Heumann, David G. George, Hans-Werner Mewes
Comput. Appl. Biosci.1