A new damage index for plane steel frames exhibiting strength and stiffness degradation under seismic motion

A new damage index for plane steel frames under earthquake ground motion is proposed. This index is defined at a section of a steel member and takes into account the interaction between the axial force N and bending moment M acting there. This interaction is defined by two curves in the N-. M plane. The first curve is the limit between elastic and inelastic material behavior, where damage is zero, while the second one is the limit between inelastic behavior and complete failure, where damage is equal to one. The damage index is defined by assuming a linear variation of damage between the two abovementioned curves. Thus, for a given N-. M combination at a member section, obtained with the aid of a two dimensional finite element program, one easily defines the damage index of that section. Material nonlinearities are taken into account by a stress-strain bilinear model including cyclic strength and stiffness degradation in the framework of lumped plasticity (plastic hinge model), while geometrical nonlinearities are modeled by including large deflection effects. The increase of damage related to strength reduction due to low-cycle fatigue is also taken into account. Several illustrative examples serve to demonstrate the use of the proposed damage index and to compare it with other well known damage indices. © 2012

Direct damage-controlled design of plane steel moment-resisting frames using static inelastic analysis

A new direct damage-controlled design method for plane steel frames under static loading is presented. Seismic loading can be handled statically in the framework of a push-over analysis. This method, in contrast to existing steel design methods, is capable of directly controlling damage, both local and global, by incorporating continuum damage mechanics for ductile materials in the analysis. The design process is accomplished with the aid of a two-dimensional finite element program, which takes into account material and geometric nonlinearities by using a nonlinear stress-strain relation through the beam-column fiber modeling and including P-δ and P-Δ effects, respectively. Simple expressions relating damage to the plastic hinge rotation of member sections and the interstorey drift ratio for three performance limit states are derived by conducting extensive parametric studies involving plane steel moment-resisting frames under static loading. Thus, a quantitative damage scale for design purposes is established. Using the proposed design method one can either determine damage for a given structure and loading, or dimension a structure for a target damage and given loading, or determine the maximum loading for a given structure and a target damage level. Several numerical examples serve to illustrate the proposed design method and demonstrate its advantages in practical applications

Translation initiation site prediction on a genomic scale : beauty in simplicity

Motivation: The correct identification of translation initiation sites (TIS) remains a challenging problem for computational methods that automatically try to solve this problem. Furthermore, the lion's share of these computational techniques focuses on the identification of TIS in transcript data. However, in the gene prediction context the identification of TIS occurs on the genomic level, which makes things even harder because at the genome level many more pseudo-TIS occur, resulting in models that achieve a higher number of false positive predictions. Results: In this article, we evaluate the performance of several 'simple' TIS recognition methods at the genomic level, and compare them to state-of-the-art models for TIS prediction in transcript data. We conclude that the simple methods largely outperform the complex ones at the genomic scale, and we propose a new model for TIS recognition at the genome level that combines the strengths of these simple models. The new model obtains a false positive rate of 0.125 at a sensitivity of 0.80 on a well annotated human chromosome ( chromosome 21). Detailed analyses show that the model is useful, both on its own and in a simple gene prediction setting

MetWAMer: eukaryotic translation initiation site prediction

<p>Abstract</p> <p>Background</p> <p>Translation initiation site (TIS) identification is an important aspect of the gene annotation process, requisite for the accurate delineation of protein sequences from transcript data. We have developed the MetWAMer package for TIS prediction in eukaryotic open reading frames of non-viral origin. MetWAMer can be used as a stand-alone, third-party tool for post-processing gene structure annotations generated by external computational programs and/or pipelines, or directly integrated into gene structure prediction software implementations.</p> <p>Results</p> <p>MetWAMer currently implements five distinct methods for TIS prediction, the most accurate of which is a routine that combines weighted, signal-based translation initiation site scores and the contrast in coding potential of sequences flanking TISs using a perceptron. Also, our program implements clustering capabilities through use of the <it>k</it>-medoids algorithm, thereby enabling cluster-specific TIS parameter utilization. In practice, our static weight array matrix-based indexing method for parameter set lookup can be used with good results in data sets exhibiting moderate levels of 5'-complete coverage.</p> <p>Conclusion</p> <p>We demonstrate that improvements in statistically-based models for TIS prediction can be achieved by taking the class of each potential start-methionine into account pending certain testing conditions, and that our perceptron-based model is suitable for the TIS identification task. MetWAMer represents a well-documented, extensible, and freely available software system that can be readily re-trained for differing target applications and/or extended with existing and novel TIS prediction methods, to support further research efforts in this area.</p

Differential impact of LPG-and PG-deficient Leishmania major mutants on the immune response of human dendritic cells

<div><p>Background</p><p><i>Leishmania major</i> infection induces robust interleukin-12 (IL12) production in human dendritic cells (hDC), ultimately resulting in Th1-mediated immunity and clinical resolution. The surface of <i>Leishmania</i> parasites is covered in a dense glycocalyx consisting of primarily lipophosphoglycan (LPG) and other phosphoglycan-containing molecules (PGs), making these glycoconjugates the likely pathogen-associated molecular patterns (PAMPS) responsible for IL12 induction.</p><p>Methodology/Principal Findings</p><p>Here we explored the role of parasite glycoconjugates on the hDC IL12 response by generating <i>L</i>. <i>major</i> Friedlin V1 mutants defective in LPG alone, (FV1 <i>lpg1-</i>), or generally deficient for all PGs, (FV1 <i>lpg2-</i>). Infection with metacyclic, infective stage, <i>L</i>. <i>major</i> or purified LPG induced high levels of <i>IL12B</i> subunit gene transcripts in hDCs, which was abrogated with FV1 <i>lpg1-</i> infections. In contrast, hDC infections with FV1 <i>lpg2-</i> displayed increased <i>IL12B</i> expression, suggesting other PG-related/<i>LPG2</i> dependent molecules may act to dampen the immune response. Global transcriptional profiling comparing WT, FV1 <i>lpg1-</i>, FV1 <i>lpg2-</i> infections revealed that FV1 <i>lpg1-</i> mutants entered hDCs in a silent fashion as indicated by repression of gene expression. Transcription factor binding site analysis suggests that LPG recognition by hDCs induces IL-12 in a signaling cascade resulting in Nuclear Factor κ B (NFκB) and Interferon Regulatory Factor (IRF) mediated transcription.</p><p>Conclusions/Significance</p><p>These data suggest that <i>L</i>. <i>major</i> LPG is a major PAMP recognized by hDC to induce IL12-mediated protective immunity and that there is a complex interplay between PG-baring <i>Leishmania</i> surface glycoconjugates that result in modulation of host cellular IL12.</p></div

Classification and Regression Tree and Spatial Analyses Reveal Geographic Heterogeneity in Genome Wide Linkage Study of Indian Visceral Leishmaniasis

Genome wide linkage studies (GWLS) have provided evidence for loci controlling visceral leishmaniasis on Chromosomes 1p22, 6q27, 22q12 in Sudan and 6q27, 9p21, 17q11-q21 in Brazil. Genome wide studies from the major focus of disease in India have not previously been reported.We undertook a GWLS in India in which a primary ∼10 cM (515 microsatellites) scan was carried out in 58 multicase pedigrees (74 nuclear families; 176 affected, 353 total individuals) and replication sought in 79 pedigrees (102 nuclear families; 218 affected, 473 total individuals). The primary scan provided evidence (≥2 adjacent markers allele-sharing LOD≥0.59; nominal P≤0.05) for linkage on Chromosomes 2, 5, 6, 7, 8, 10, 11, 20 and X, with peaks at 6p25.3-p24.3 and 8p23.1-p21.3 contributed to largely by 31 Hindu families and at Xq21.1-q26.1 by 27 Muslim families. Refined mapping confirmed linkage across all primary scan families at 2q12.2-q14.1 and 11q13.2-q23.3, but only 11q13.2-q23.3 replicated (combined LOD = 1.59; P = 0.0034). Linkage at 6p25.3-p24.3 and 8p23.1-p21.3, and at Xq21.1-q26.1, was confirmed by refined mapping for primary Hindu and Muslim families, respectively, but only Xq21.1-q26.1 replicated across all Muslim families (combined LOD 1.49; P = 0.0045). STRUCTURE and SMARTPCA did not identify population genetic substructure related to religious group. Classification and regression tree, and spatial interpolation, analyses confirm geographical heterogeneity for linkages at 6p25.3-p24.3, 8p23.1-p21.3 and Xq21.1-q26.1, with specific clusters of families contributing LOD scores of 2.13 (P = 0.0009), 1.75 (P = 0.002) and 1.84 (P = 0.001), respectively.GWLS has identified novel loci that show geographical heterogeneity in their influence on susceptibility to VL in India

Erratum: Corrigendum: Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution

International Chicken Genome Sequencing Consortium. The Original Article was published on 09 December 2004. Nature432, 695–716 (2004). In Table 5 of this Article, the last four values listed in the ‘Copy number’ column were incorrect. These should be: LTR elements, 30,000; DNA transposons, 20,000; simple repeats, 140,000; and satellites, 4,000. These errors do not affect any of the conclusions in our paper. Additional information. The online version of the original article can be found at 10.1038/nature0315