Distributed Management of Massive Data: an Efficient Fine-Grain Data Access Scheme

This paper addresses the problem of efficiently storing and accessing massive data blocks in a large-scale distributed environment, while providing efficient fine-grain access to data subsets. This issue is crucial in the context of applications in the field of databases, data mining and multimedia. We propose a data sharing service based on distributed, RAM-based storage of data, while leveraging a DHT-based, natively parallel metadata management scheme. As opposed to the most commonly used grid storage infrastructures that provide mechanisms for explicit data localization and transfer, we provide a transparent access model, where data are accessed through global identifiers. Our proposal has been validated through a prototype implementation whose preliminary evaluation provides promising results

Optimization in a Self-Stabilizing Service Discovery Framework for Large Scale Systems

Ability to find and get services is a key requirement in the development of large-scale distributed sys- tems. We consider dynamic and unstable environments, namely Peer-to-Peer (P2P) systems. In previous work, we designed a service discovery solution called Distributed Lexicographic Placement Table (DLPT), based on a hierar- chical overlay structure. A self-stabilizing version was given using the Propagation of Information with Feedback (PIF) paradigm. In this paper, we introduce the self-stabilizing COPIF (for Collaborative PIF) scheme. An algo- rithm is provided with its correctness proof. We use this approach to improve a distributed P2P framework designed for the services discovery. Significantly efficient experimental results are presented

The Worm-Specific Immune Response in Multiple Sclerosis Patients Receiving Controlled Trichuris suis Ova Immunotherapy

Considering their potent immunomodulatory properties, therapeutic applications of Trichuris suis ova (TSO) are studied as potential alternative treatment of autoimmune disorders like multiple sclerosis (MS), rheumatoid arthritis (RA), or inflammatory bowel disease (IBD). Clinical phase 1 and 2 studies have demonstrated TSO treatment to be safe and well tolerated in MS patients, however, they reported only modest clinical efficacy. We therefore addressed the cellular and humoral immune responses directed against parasite antigens in individual MS patients receiving controlled TSO treatment (2500 TSO p.o. every 2 weeks for 12 month). Peripheral blood mononuclear cells (PBMC) of MS patients treated with TSO (n = 5) or placebo (n = 6) were analyzed. A continuous increase of serum IgG and IgE antibodies specific for T. suis excretory/secretory antigens was observed up to 12 months post-treatment. This was consistent with mass cytometry analysis identifying an increase of activated HLA-DRhigh plasmablast frequencies in TSO-treated patients. While stable and comparable frequencies of total CD4+ and CD8+ T cells were detected in placebo and TSO-treated patients over time, we observed an increase of activated HLA-DR+CD4+ T cells in TSO-treated patients only. Frequencies of Gata3+ Th2 cells and Th1/Th2 ratios remained stable during TSO treatment, while Foxp3+ Treg frequencies varied greatly between individuals. Using a T. suis antigen-specific T cell expansion assay, we also detected patient-to-patient variation of antigen-specific T cell recall responses and cytokine production. In summary, MS patients receiving TSO treatment established a T. suis-specific T- and B-cell response, however, with varying degrees of T cell responses and cellular functionality across individuals, which might account for the overall miscellaneous clinical efficacy in the studied patients

DIET : new developments and recent results

Among existing grid middleware approaches, one simple, powerful, and flexibleapproach consists of using servers available in different administrative domainsthrough the classic client-server or Remote Procedure Call (RPC) paradigm.Network Enabled Servers (NES) implement this model also called GridRPC.Clients submit computation requests to a scheduler whose goal is to find aserver available on the grid. The aim of this paper is to give an overview of anNES middleware developed in the GRAAL team called DIET and to describerecent developments. DIET (Distributed Interactive Engineering Toolbox) is ahierarchical set of components used for the development of applications basedon computational servers on the grid.Parmi les intergiciels de grilles existants, une approche simple, flexible et performante consiste a utiliser des serveurs disponibles dans des domaines administratifs différents à travers le paradigme classique de l’appel de procédure àdistance (RPC). Les environnements de ce type, connus sous le terme de Network Enabled Servers, implémentent ce modèle appelé GridRPC. Des clientssoumettent des requêtes de calcul à un ordonnanceur dont le but consiste àtrouver un serveur disponible sur la grille.Le but de cet article est de donner un tour d’horizon d’un intergiciel développédans le projet GRAAL appelé DIET 1. DIET (Distributed Interactive Engineering Toolbox) est un ensemble hiérarchique de composants utilisés pour ledéveloppement d’applications basées sur des serveurs de calcul sur la grille

FASTLens (FAst STatistics for weak Lensing) : Fast method for Weak Lensing Statistics and map making

With increasingly large data sets, weak lensing measurements are able to measure cosmological parameters with ever greater precision. However this increased accuracy also places greater demands on the statistical tools used to extract the available information. To date, the majority of lensing analyses use the two point-statistics of the cosmic shear field. These can either be studied directly using the two-point correlation function, or in Fourier space, using the power spectrum. But analyzing weak lensing data inevitably involves the masking out of regions or example to remove bright stars from the field. Masking out the stars is common practice but the gaps in the data need proper handling. In this paper, we show how an inpainting technique allows us to properly fill in these gaps with only $N \log N$ operations, leading to a new image from which we can compute straight forwardly and with a very good accuracy both the pow er spectrum and the bispectrum. We propose then a new method to compute the bispectrum with a polar FFT algorithm, which has the main advantage of avoiding any interpolation in the Fourier domain. Finally we propose a new method for dark matter mass map reconstruction from shear observations which integrates this new inpainting concept. A range of examples based on 3D N-body simulations illustrates the results.Comment: Final version accepted by MNRAS. The FASTLens software is available from the following link : http://irfu.cea.fr/Ast/fastlens.software.ph

New tools and methods for direct programmatic access to the dbSNP relational database

Genome-wide association studies often incorporate information from public biological databases in order to provide a biological reference for interpreting the results. The dbSNP database is an extensive source of information on single nucleotide polymorphisms (SNPs) for many different organisms, including humans. We have developed free software that will download and install a local MySQL implementation of the dbSNP relational database for a specified organism. We have also designed a system for classifying dbSNP tables in terms of common tasks we wish to accomplish using the database. For each task we have designed a small set of custom tables that facilitate task-related queries and provide entity-relationship diagrams for each task composed from the relevant dbSNP tables. In order to expose these concepts and methods to a wider audience we have developed web tools for querying the database and browsing documentation on the tables and columns to clarify the relevant relational structure. All web tools and software are freely available to the public at http://cgsmd.isi.edu/dbsnpq. Resources such as these for programmatically querying biological databases are essential for viably integrating biological information into genetic association experiments on a genome-wide scale

Systematic Comparison of Three Methods for Fragmentation of Long-Range PCR Products for Next Generation Sequencing

Next Generation Sequencing (NGS) technologies are gaining importance in the routine clinical diagnostic setting. It is thus desirable to simplify the workflow for high-throughput diagnostics. Fragmentation of DNA is a crucial step for preparation of template libraries and various methods are currently known. Here we evaluated the performance of nebulization, sonication and random enzymatic digestion of long-range PCR products on the results of NGS. All three methods produced high-quality sequencing libraries for the 454 platform. However, if long-range PCR products of different length were pooled equimolarly, sequence coverage drastically dropped for fragments below 3,000 bp. All three methods performed equally well with regard to overall sequence quality (PHRED) and read length. Enzymatic fragmentation showed highest consistency between three library preparations but performed slightly worse than sonication and nebulization with regard to insertions/deletions in the raw sequence reads. After filtering for homopolymer errors, enzymatic fragmentation performed best if compared to the results of classic Sanger sequencing. As the overall performance of all three methods was equal with only minor differences, a fragmentation method can be chosen solely according to lab facilities, feasibility and experimental design

Shutdown Policies with Power Capping for Large Scale Computing Systems

International audienceLarge scale distributed systems are expected to consume huge amounts of energy. To solve this issue, shutdown policies constitute an appealing approach able to dynamically adapt the resource set to the actual workload. However, multiple constraints have to be taken into account for such policies to be applied on real infrastructures, in particular the time and energy cost of shutting down and waking up nodes, and power capping to avoid disruption of the system. In this paper, we propose models translating these various constraints into different shutdown policies that can be combined. Our models are validated through simulations on real workload traces and power measurements on real testbeds.

A Mild Form of SLC29A3 Disorder: A Frameshift Deletion Leads to the Paradoxical Translation of an Otherwise Noncoding mRNA Splice Variant

We investigated two siblings with granulomatous histiocytosis prominent in the nasal area, mimicking rhinoscleroma and Rosai-Dorfman syndrome. Genome-wide linkage analysis and whole-exome sequencing identified a homozygous frameshift deletion in SLC29A3, which encodes human equilibrative nucleoside transporter-3 (hENT3). Germline mutations in SLC29A3 have been reported in rare patients with a wide range of overlapping clinical features and inherited disorders including H syndrome, pigmented hypertrichosis with insulin-dependent diabetes, and Faisalabad histiocytosis. With the exception of insulin-dependent diabetes and mild finger and toe contractures in one sibling, the two patients with nasal granulomatous histiocytosis studied here displayed none of the many SLC29A3-associated phenotypes. This mild clinical phenotype probably results from a remarkable genetic mechanism. The SLC29A3 frameshift deletion prevents the expression of the normally coding transcripts. It instead leads to the translation, expression, and function of an otherwise noncoding, out-of-frame mRNA splice variant lacking exon 3 that is eliminated by nonsense-mediated mRNA decay (NMD) in healthy individuals. The mutated isoform differs from the wild-type hENT3 by the modification of 20 residues in exon 2 and the removal of another 28 amino acids in exon 3, which include the second transmembrane domain. As a result, this new isoform displays some functional activity. This mechanism probably accounts for the narrow and mild clinical phenotype of the patients. This study highlights the ‘rescue’ role played by a normally noncoding mRNA splice variant of SLC29A3, uncovering a new mechanism by which frameshift mutations can be hypomorphic

SPOT: a web-based tool for using biological databases to prioritize SNPs after a genome-wide association study

SPOT (http://spot.cgsmd.isi.edu), the SNP prioritization online tool, is a web site for integrating biological databases into the prioritization of single nucleotide polymorphisms (SNPs) for further study after a genome-wide association study (GWAS). Typically, the next step after a GWAS is to genotype the top signals in an independent replication sample. Investigators will often incorporate information from biological databases so that biologically relevant SNPs, such as those in genes related to the phenotype or with potentially non-neutral effects on gene expression such as a splice sites, are given higher priority. We recently introduced the genomic information network (GIN) method for systematically implementing this kind of strategy. The SPOT web site allows users to upload a list of SNPs and GWAS P-values and returns a prioritized list of SNPs using the GIN method. Users can specify candidate genes or genomic regions with custom levels of prioritization. The results can be downloaded or viewed in the browser where users can interactively explore the details of each SNP, including graphical representations of the GIN method. For investigators interested in incorporating biological databases into a post-GWAS SNP selection strategy, the SPOT web tool is an easily implemented and flexible solution