122 research outputs found

    A general Dixmier trace formula for the density of states on open manifolds

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    We give an abstract formulation of the Dixmier trace formula for the density of states. This recovers prior versions and allows us to provide a Dixmier trace formula for the density of states of second order elliptic differential operators on manifolds of bounded geometry satisfying a certain geometric condition. This formula gives a new perspective on Roe's index on open manifolds.Comment: 31 pages, no figure

    MRS: a fast and compact retrieval system for biological data

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    The biological data explosion of the ‘omics’ era requires fast access to many data types in rapidly growing data banks. The MRS server allows for very rapid queries in a large number of flat-file data banks, such as EMBL, UniProt, OMIM, dbEST, PDB, KEGG, etc. This server combines a fast and reliable backend with a very user-friendly implementation of all the commonly used information retrieval facilities. The MRS server is freely accessible at . Moreover, the MRS software is freely available at for those interested in making their own data banks available via a web-based server

    Fairness in smart grid congestion management

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    With the energy transition, grid congestion is increasingly becoming a problem. This paper proposes the implementation of fairness in congestion management by presenting quantitative fair optimization goals and fairness measuring tools. Furthermore, this paper presents a congestion management solution in the form of an egalitarian allocation mechanism. Finally, this paper proves that this mechanism is truthful, pareto efficient, and maximizes a fair optimization goal

    Signature, a web server for taxonomic characterization of sequence samples using signature genes

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    Signature genes are genes that are unique to a taxonomic clade and are common within it. They contain a wealth of information about clade-specific processes and hold a strong evolutionary signal that can be used to phylogenetically characterize a set of sequences, such as a metagenomics sample. As signature genes are based on gene content, they provide a means to assess the taxonomic origin of a sequence sample that is complementary to sequence-based analyses. Here, we introduce Signature (http://www.cmbi.ru.nl/signature), a web server that identifies the signature genes in a set of query sequences, and therewith phylogenetically characterizes it. The server produces a list of taxonomic clades that share signature genes with the set of query sequences, along with an insightful image of the tree of life, in which the clades are color coded based on the number of signature genes present. This allows the user to quickly see from which part(s) of the taxonomy the query sequences likely originate

    Protein structure analysis of mutations causing inheritable diseases. An e-Science approach with life scientist friendly interfaces

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    Contains fulltext : 89590.pdf (publisher's version ) (Open Access)BACKGROUND: Many newly detected point mutations are located in protein-coding regions of the human genome. Knowledge of their effects on the protein's 3D structure provides insight into the protein's mechanism, can aid the design of further experiments, and eventually can lead to the development of new medicines and diagnostic tools. RESULTS: In this article we describe HOPE, a fully automatic program that analyzes the structural and functional effects of point mutations. HOPE collects information from a wide range of information sources including calculations on the 3D coordinates of the protein by using WHAT IF Web services, sequence annotations from the UniProt database, and predictions by DAS services. Homology models are built with YASARA. Data is stored in a database and used in a decision scheme to identify the effects of a mutation on the protein's 3D structure and function. HOPE builds a report with text, figures, and animations that is easy to use and understandable for (bio)medical researchers. CONCLUSIONS: We tested HOPE by comparing its output to the results of manually performed projects. In all straightforward cases HOPE performed similar to a trained bioinformatician. The use of 3D structures helps optimize the results in terms of reliability and details. HOPE's results are easy to understand and are presented in a way that is attractive for researchers without an extensive bioinformatics background

    Fairness in Power Flow Network Congestion Management with Outer Matching and Principal Notions of Fair Division

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    The problem of network flow congestion occurring in power networks is increasing in severity. Especially in low-voltage networks this is a novel development. The congestion is caused for a large part by distributed and renewable energy sources introducing a complex blend of prosumers to the network. Since congestion management solutions may require individual prosumers to alter their prosumption, the concept of fairness has become a crucial topic of attention. This paper presents a concept of fairness for low-voltage networks that prioritizes local, outer matching and allocates grid access through fair division of available capacity. Specifically, this paper discusses three distinct principal notions of fair division; proportional, egalitarian, and nondiscriminatory division. In addition, this paper devises an efficient algorithmic mechanism that computes such fair allocations in limited computational time, and proves that only egalitarian division results in incentive compatibility of the mechanism

    ValiDichro: a website for validating and quality control of protein circular dichroism spectra

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    Circular dichroism (CD) spectroscopy is widely used in structural biology as a technique for examining the structure, folding and conformational changes of proteins. A new server, ValiDichro, has been developed for checking the quality and validity of CD spectral data and metadata, both as an aid to data collection and processing and as a validation procedure for spectra to be included in publications. ValiDichro currently includes 25 tests for data completeness, consistency and quality. For each test that is done, not only is a validation report produced, but the user is also provided with suggestions for correcting or improving the data. The ValiDichro server is freely available at http://valispec.cryst.bbk.ac.uk/circularDichroism/ValiDichro/upload.html

    WIWS: a protein structure bioinformatics Web service collection

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    The WHAT IF molecular-modelling and drug design program is widely distributed in the world of protein structure bioinformatics. Although originally designed as an interactive application, its highly modular design and inbuilt control language have recently enabled its deployment as a collection of programmatically accessible web services. We report here a collection of WHAT IF-based protein structure bioinformatics web services: these relate to structure quality, the use of symmetry in crystal structures, structure correction and optimization, adding hydrogens and optimizing hydrogen bonds and a series of geometric calculations. The freely accessible web services are based on the industry standard WS-I profile and the EMBRACE technical guidelines, and are available via both REST and SOAP paradigms. The web services run on a dedicated computational cluster; their function and availability is monitored daily

    A series of PDB related databases for everyday needs

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    The Protein Data Bank (PDB) is the world-wide repository of macromolecular structure information. We present a series of databases that run parallel to the PDB. Each database holds one entry, if possible, for each PDB entry. DSSP holds the secondary structure of the proteins. PDBREPORT holds reports on the structure quality and lists errors. HSSP holds a multiple sequence alignment for all proteins. The PDBFINDER holds easy to parse summaries of the PDB file content, augmented with essentials from the other systems. PDB_REDO holds re-refined, and often improved, copies of all structures solved by X-ray. WHY_NOT summarizes why certain files could not be produced. All these systems are updated weekly. The data sets can be used for the analysis of properties of protein structures in areas ranging from structural genomics, to cancer biology and protein design
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