Posters
Category 'Q'- Other' |
Poster - Q01 |
FluxCTTX: A LIMS-Based Tool for Management and Analysis of Cytotoxicity Assays Data |
Alessandra Faria-Campos, Federal University of Minas Gerais, Brazil |
Luciene Balottin, INMETRO, Brazil Gianlucca Zuin, UFMG, Brazil Vinicius Garcia, UFMG, Brazil Paulo Henrique Batista, UFMG, Brazil José Mauro Granjeiro, INMETRO, Brazil Sérgio Vale Aguiar Campos, UFMG, Brazil |
Short Abstract: This work describes the development of FluxCTTX, a tool for management of data from cytotoxicity assays described in the OECD129 Guidance Document. The main work is the development of a workflow, which represents all stages of the assay and is uploaded in a LIMS. The workflow models all assay activities. |
Poster - Q02 |
Development of a automated system for management and analysis of data from meningitis patients |
Philippe Menezes, Universidade Federal de Minas Gerais, Brazil |
Vinícius Garcia, Universidade Federal de Minas Gerais, Brazil Bárbara Mata, Centro de Pesquisas René Rachou, Brazil Natália Arantes, Universidade Federal de Minas Gerais, Brazil Roney Coimbra, Centro de Pesquisas René Rachou, Brazil Alessandra Campos, Universidade Federal de Minas Gerais, Brazil Sérgio Campos, Universidade Federal de Minas Gerais, Brazil |
Short Abstract: Several data regarding the patient is generated to diagnose meningitis. These data are generally organized in medical paper forms which are difficult to manage and analyze. A workflow was created to storage the data from patients, allowing the data to be managed and analysed in a effective and organized manner. |
Poster - Q03 |
NRDR 2.0: New database, Novel Knowledge |
Pedro Borges, Federal University of Technology, Paraná - Cornelio Procópio, PR, Brazil, Brazil |
Alexandre Paschoal, Federal University of Technology, Paraná - Cornelio Procópio, PR, Brazil., Brazil Vinícius Maracajá-Coutinho, Bioinformatics Core, Centro de Genómica y Bioinformática, Universidad Mayor, Chile João Setubal, Instituto de Química, Universidade de São Paulo, Brazil Sérgio Verjovski-Almeida, Instituto de Química, Universidade de São Paulo, Brazil Zilá Simões, Faculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Brazil Alan Michell, Ciência da Computação, Instituto de Matemática e Estatística, Universidade de São Paulo, Brazil |
Short Abstract: We present NRDR 2.0 (www.ncrnadatabases.org) - Non-coding RNA Database Resource – a repository for non-coding RNA database knowledge. The main goal is to provide an effective way of searching for the ncRNA information available in the web. NRDR 2.0 indexes 140 databases (an increase of 37% compared to NRDR 1. |
Poster - Q04 |
MODELING RNA SECONDARY STRUCTURE CONSIDERING TRANSCRIPTIONAL PAUSING EFFECTS |
Pedro Costa, Instituto de Biociências de Botucatu, Brazil |
Ney Lemke, IBB - Unesp, Brazil |
Short Abstract: Predicting the folding pathway for the native and active structures of functional noncoding RNAs from primary RNA sequence remains a challenge for biophysicists and computational biologists. We propose a heuristic approach to study the effects of transcriptional pausing on RNA. |
Poster - Q05 |
Development of workflows for a LIMS to support the adherence to Good Laboratory Practices |
Handressa Feu, INMETRO, Brazil |
Alessandra Faria-Campos, INMETRO, Brazil Aurea Folgueras-Flatschart, INMETRO, Brazil Sérgio Campos, Universidade Federal de Minas Gerais, Brazil José Mauro Granjeiro, INMETRO, Brazil |
Short Abstract: Development of a set of workflows to be used in the LIMS Flux, that adapts to different laboratories, to be used to support adherence to GLP principles. |
Poster - Q06 |
NRDR 2.0: New database, Novel Knowledge |
Pedro Borges, Federal University of Technology - Paraná, Brazil |
Alexandre Paschoal Federal University of Technology - Paraná, Brazil Pedro Borges, Federal University of Technology - Paraná, Brazil Flavia Sabino, Embrapa-Soja, Brazil Sibele de Souza, USP, Brazil Raul Arias-Carrasco, Centro de Genómica y Bioinformática, Universidad Mayor, Chile Vinicius Maracajá-Coutinho, Centro de Genómica y Bioinformática, Universidad Mayor, Chile Artur Queiroz, FIOCRUZ-BA, Brazil Liliane Santana, Albert Einstein Research and Education Institute, Hospital Israelita Albert Einstein, Sao Paulo, Brazil Douglas Domingues, IAPAR, Brazil João Carlos Setubal, Instituto de Química, Universidade de São Paulo, Brazil Zilá Simões, Faculdade de Filosofia Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, Brazil Sergio Verjovski-Almeida, Instituto de Química, Universidade de São Paulo, Brazil Alan Durham, Instituto de Matemática e Estatística, Universidade de São Paulo, Brazil |
Short Abstract: We present NRDR 2.0 - Non-coding RNA Database Resource – a repository for non-coding RNA database knowledge. The main goal of NRDR (www.ncrnadatabases.org) is to provide an effective way of searching for the ncRNA information available in the web. We have created a classification system that enables users to quickly locate the available data sources they need. This involves manual curation of each of the internet resources to classify the information stored and the availability of the data. Researchers can search the available web ncRNA databases based on information source (experimental, manually curated, in silico prediction, literature), information content, RNA Family, availability of data for download, search methods available, organisms. Additionally there is a free text search option based on words extracted from the database descriptions. NRDR 2.0 currently indexes 140 databases (an increase of 37% when compared to NRDR 1.0). Each of the 140 databases described in NRDR were manually analyzed by a curator and all information was carefully extracted. Additionally, NRDR also includes a database of more than 8 million ncRNA sequences extracted from 30 different internet resources. The sequences in this database can be downloaded and also can be searched by species or with a BLAST similarity search. NRDR 2.0 is now maintained by a team composed by 13 academics (professors, post docs and graduate students) from 7 institutions to guarantee that all data stored is manually curated before its inclusion. The search options of the database can be used not only to search ncRNA information, but also to have a picture of the research in the area. To the best of our knowledge, there is no other resource available that offers such comprehensive integration and search possibilities. |
Poster - Q07 |
Study and Comparison of Heuristics for the Problem of Genome Rearrangement by Unsigned Reversals |
Eduardo Fernandes, Universidade Federal de Mato Grosso do Sul, Brazil |
Eloi Araujo, Universidade Federal de Mato Grosso do Sul, Brazil |
Short Abstract: Genome rearrangement is a problem in computational molecular biology that can be described as a succession of changes on a chromosome, specifically in the order of blocks of gene in a sequence of the chromosome. One of the variants of the problem is known as genome rearrangement by unsigned reversals. The main goal of this work is to study this specific problem. A chromosome can be represented by a permutation, that is a sequence of genes in which each gene is indicated by integers. The problem of genome rearrangement by reversals consists in sorting the genes of a sequence using the smallest amount of operations known as reversals. An unsigned reversal, or simply reversal, is defined as an operation that reverses the order of genes in a range of the sequence. Genome rearrangement problem is difficult because there is no polynomial algorithms for them unless P = NP. This work consists of: the theoretical study of a sorting algorithm by reversing previously described; the proposal of some new heuristics; and the comparison among the implemented algorithms. Basically, there are four heuristics that were studied in this work, one of them is from literature and the other three were proposed by us. All the algorithms were implemented using C++ language and executed in the supercomputer of the Technological Center of Electronics and Computer (Centro Tecnológico de Eletrônica e Informática – CTEI), at the Federal University of Mato Grosso do Sul (UFMS), using a set of random entries with different sizes. |
Poster - Q08 |
Unraveling evolutionary pathways for genomic and phenotypic diversification and its predicted impact on the ecophysiology of biomining Acidithiobacilli |
Carolina González, Fundación Ciencia & Vida y Facultad de Ciencias Biológicas; Fraunhofer Chile Research Foundation - Center for Systems Biotechnology, Chile |
Darwin Guzmán, Fraunhofer Chile Research Foundation - Center for Systems Biotechnology, Chile Paz Tapia, Fraunhofer Chile Research Foundation - Center for Systems Biotechnology, Chile David Holmes, Fundación Ciencia & Vida y Facultad de Ciencias Biológicas, Universidad Andrés Bello, Chile Jorge Valdés, Fraunhofer Chile Research Foundation - Center for Systems Biotechnology, Chile |
Short Abstract: Members of the Acidithiobacillus genus are well characterized for their ability to obtain energy from inorganic sources in extreme acidic environments and their application in metal recovery. This work aids to the understanding of evolutionary processes that have shaped the current genomic structure and phenotypic properties of Acidithiobacillus representatives. |
Poster - Q09 |
Homebox and DNA repeats: two coordinate elements in the human genome |
Fabian Tobar Tosse, Pontificia Universidad Javeriana Cali, Colombia |
Eliana Ocampo Toro, Pontificia Universidad Javeriana Cali, Colombia |
Short Abstract: Homeobox gene family and DNA repeats are important elements for the regulation of the gene expression, herein we present a network of association among these elements from the human genome, and the relationship of these connections with biological processes. |
Poster - Q10 |
Aldehyde oxidoreductase from Desulfovibrio gigas: Characterization of the electron transfer chain between Mo and the proximal FeS center by EPR and DFT studies |
María Gómez, Facultad de Bioquímica y Ciencias Biológicas Universidad Nacional del Litoral, Argentina |
Nicolas Neuman, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Argentina Pablo Gonzalez, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Argentina Alberto Rizzi, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Argentina Carlos Brondino, Facultad de Bioquímica y Ciencias Biológicas, Universidad Nacional del Litoral, Argentina Sergio Dalosto, CONICET, Argentina |
Short Abstract: We report here EPR studies complemented with first-principles computational simulations of reduced as-purified and glycerol-(GOL), and ethylene glycol-(EDO)inhibited DgAOR. We evaluate the exchange parameter J between FeS 1 and Mo in distinct situations and correlate the changes in J with the spin density on the Mo atom upon alcohol inhibition |
Poster - Q11 |
Inhibitors of the Malato-Synthase Enzyme of Paracoccidioides spp: Receptor-ligand interaction-based virtual screening and molecular docking studies |
Fausto Costa, Universidade Federal de Goías, Brazil |
Ricardo Lemes Gonçalves, Universidade Federal de Goiás, Brazil Lucília Kato, Universidade Federal de Goiás, Brazil Cecília Maria Alves de Oliveira, Universidade Federal de Goiás, Brazil Célia Maria de Almeida Soares, Universidade Federal de Goiás, Brazil Benedito Rodrigues da Silva Neto, Universidade Federal de Goiás, Brazil Maristela Pereira, Universidade Federa de Goiás, Brazil Roosevelt Alves da Silva, Universidade Federal de Goiás, Brazil |
Short Abstract: The Malate-Synthase of Paracoccidioides brasiliensis is a key enzyme of the glyoxylate pathway and play a crucial role in the pathogenicity this microorganism. PbMLS is considered a therapeutic target for the development of novel antifungal compounds able to treat this disease. This proposal aims to select compounds with affinity to this enzyme. |
Poster - Q12 |
eQTL study of RPBs gene expression |
Fernando Andrade, University of São Paulo, Brazil |
André Fujita, University of São Paulo, Brazil |
Short Abstract: This work assess the regulation of RNA binding proteins, proteins that a crucial to the regulation of tranlation in cells. Using eQTL we try to decipher their regulatory architecture. |
Poster - Q13 |
How This Database can Impact New Vaccine Strategies Development |
gustavo vieira, Universidade Federal do Rio Grande do Sul, Brazil |
Marialva Sinigaglia, UFRGS, Brazil Mauricio Rigo, UFRGS, Brazil Dinler Antunes, UFRGS, Brazil Marcus Mendes, UFRGS, Brazil Martiela Freitas, UFRGS, Brazil Renata Tarabini, UFRGS, Brazil Marcelo Bragatte, UFRGS, Brazil |
Short Abstract: CrossTope opens a new way for the exploration of immunogenic epitopes and the comparison at the strucstural level. Our project intend to allow researchers from all over the world to create their customized 3D epitopes (pMHC) in a fast and low cost way. |
Poster - Q14 |
Sequencing, assembly and annotation of Burkholderia sacchari genome for reconstruction of metabolic network involved in bioplastic production |
Paulo Alexandrino, University of São Paulo, Brazil |
Thatiane Mendonça, University of São Paulo, Brazil Linda Bautista, University of São Paulo, Brazil Juliano Cherix, University of São Paulo, Brazil Gabriela Lozano, University of São Paulo, Brazil Edmar Filho, University of São Paulo, Brazil Marilda Taciro, University of São Paulo, Brazil José Gomez, University of São Paulo, Brazil Luiziana Silva, University of São Paulo, Brazil André Fujita, University of São Paulo, Brazil |
Short Abstract: Burkholderia sacchari is a natural bioplastic producer bacteria with relevant industrial aspect. Genome information is extremely helpful to guide metabolic analysis and to evaluate bacterial potential. In this work, we have sequenced Burkholderia sacchari genome for the first time, annotated it and then created a metabolic model for bioplastic production. |
Poster - Q15 |
Whole-genome analysis of Pasteurella multocida strain Alpaca to identify potential vaccine candidates against acute pneumonia |
Eduardo Juscamayta, UNMSM, Peru |
Lenin Maturrano University of San Marcos, Peru Eduardo Juscamayta, UNMSM, Peru Daniel Fernandez, UNMSM, Peru Raquel Hurtado, UNMSM, Peru Nataly Allasi, UNMSM, Peru Raul Rosadio, UNMSM, Peru |
Short Abstract: For us, the ISCB-LA 2014 is the most important summit on Bioinformatics and Genomics, and we would like to attend this event to show our research in genomics of pathogens of alpacas. Also we would like to know and put in contact with research groups in this area |
Poster - Q16 |
Whole Genome Sequencing and Comparative Analysis of Pasteurella multocida Strain UNMSM isolate from Alpaca |
Raquel Hurtado, UNMSM, Peru |
Lenin Maturrano University of San Marcos, Peru Eduardo Juscamayta, UNMSM, Peru Daniel Fernandez, UNMSM, Peru Raquel Hurtado, UNMSM, Peru Nataly Allasi, UNMSM, Peru |
Short Abstract: Pasteurella multocida is considered the main etiological agent of acute pneumonia in alpacas and the main mortality causes in young alpacas in Peru. For that reason, we sequenced the complete genome of P. multocida strain UNMSM, and we report the whole-genome sequence from a strain isolated from acute pneumonias |
Poster - Q17 |
A sophisticated computational method to study protein dynamics and to complement EPR data. A study on conformational dynamics of photosynthetic reaction center of Rb. spheroides |
MNV Prasad Gajula, Institute of Biotechnology, India |
Igor Borovykh, University of osnabrueckj, Germany HJ Steinhoff, University of osnabrueckj, Germany Peter Gast, leiden university, Netherlands Anuj Kumar, Meerut University , India PA Kumar, Institute of bioechnology, India ea Siddiq, Institute of bioechnology, India |
Short Abstract: None On File |
Poster - Q18 |
Displacement of the tyrosyl radical in RNR enzyme: a novel computational approach to analyze EPR experimental data |
MNVP Gajula, Institute of Biotechnology, India |
HJ Steinhoff, University of Osnabrueck, Germany Anuj Kumar, Meerut University, India EA Siddiq, Institute of Biotechnology, India PA Kumar, Institute of Biotechnology, India Friedhelm Lendzian, Technical University Berlin, Germany |
Short Abstract: None On File |
Poster - Q19 |
Integrative network-based approach identifies key genetic elements in breast invasive carcinoma |
Mohamed Hamed, Saarland University, Germany |
Christian Spaniol, Saarland University, Germany Alexander Zapp, Saarland University, Germany Volkhard Helms, Saarland University, Germany |
Short Abstract: None On File |
Poster - Q20 |
Developing New Strategies for Protein Structure Prediction |
Muhammad Rizwan Riaz, COMSATS Institute of Information Technology, Pakistan |
Abdul Rauf Siddiqi, COMSATS Institute of Information Technology islamabad, Pakistan |
Short Abstract: Determining the 3D structure of protein is an important problem for biologists. Because of gap between number of experimentally solved structures and known protein sequences, it becomes difficult to model the structure of proteins by conventional modeling methods. Proposed Methodology helps biologist to overcome this problem by using hybrid technique. |
Poster - Q21 |
Molecular modeling of protein CovR of streptococcus mutans- a promising target against human cariogenesis |
Nelson Nascimento de Alencar, Faculdade Integrada Brasil Amazônia - FIBRA, Brazil |
Jonas França Cruz, FIBRA, Brazil Adonis Lima, FIBRA, Brazil Ronaldo Silva, FIBRA, Brazil |
Short Abstract: Streptococcus mutans is the main pathogen of dental caries in humans,is involved in the etiology of bacterial endocarditis. In this study, the 3D structure of CovR has been determined by homology. the result obtained was validated considering the RMSD, Molprobity and ANOLEA. The modeling showed consistency with known experimental data |
Poster - Q22 |
SMAR genomic elements: toward a signature to in silico prediction of these epigenetic regulators |
Newton Verbisck, Embrapa Beef Cattle, Brazil |
Short Abstract: INTRODUCTION: The eukaryotic chromosomal DNA is attached to the nuclear proteinaceous scaffold/matrix by genomic elements known as SMAR (Scaffold/Matrix Attachment Regions). SMAR elements have been characterized as non-coding short DNA sequences (100 to 3000 base pairs) able to enhance transcriptional activity and prevent position effect variegation of transgenes (1,2). Even though several structural motifs have been assigned to SMAR elements, no consensus sequences or sequence motifs exclusively associated to them have already been characterized. A computational analysis allowed the isolation of mouse genome SMARs, which resulted to be powerful activators of transgene expression in stable transfections (3). Here we report another in silico analysis of SMAR DNA sequences and the finding that a combination of motifs has the potential to be used as a new signature to predict these genomic elements. MATERIALS AND METHODS: Comparative analysis of 34 associated SMAR motifs was performed over 11 well characterized SMAR sequences available at GenBank and SMARt databases. Motif assignment was done with freely available text editor software. CpGPlot at EMBOSS website was used to find CpG islands within the sequences. RESULTS AND CONCLUSION: We have found that only 9 motifs are common to all SMAR sequences studied. These motifs were used to build maps that have revealed a pattern obtained with only 5 motifs, including SMAR recognition rules formerly described by other groups (4,5). We observed an ordered position distribution for those 5 motifs despite that the distance between them has varied considerably within all the different SMARs studied. The array of these motifs can be putatively ascribed as a SMAR signature and used to perform future SMAR genomic prediction more successfully. 1. Linnemann et al, Biochem Soc Trans, 35, 612-7, 2007. 2. Galbete et al, Mol Biosyst, 5, 143-50, 2009. 3. Harraghy et al, J Biotech, 125, 11-20, 2011. 4. Girod & Mermod, S. C. Makrides (Ed.) Gene Transfer and Expression in Mammalian Cells, Ch. 10, 2003. 5. Singh et al, Nucleic Acids Res, 25, 1419-25, 1997. |
Poster - Q23 |
Inference Of Regulatory Networks With A Convergence Improved Markov Chain Monte Carlo Sampler |
Nilzair Agostinho, Universidade Federal do Rio Grande (FURG), Brazil |
Adriano Werhli, FURG, Brazil Karina Machado, FURG, Brazil |
Short Abstract: Bayesian networks (BN) are promising for the inference of regulatory networks and usually are sampled with a Markov Chain Monte Carlo (MCMC) (often slow in convergence). The proposed method combines Graphical Gaussian Models, with the BN model in order to improve the mixing and convergence of the MCMC. |
Poster - Q24 |
MISSIONN-T2D: a multi-scale model for the onset of type 2 diabetes |
Paolo Tieri, Consiglio Nazionale delle Ricerche, Italy |
Filippo Castiglione, CNR, Italy Albert De Graaf, TNO, Netherlands Claudio Franceschi, Univ Bologna, Italy Pietro Liò, Univ Cambirdge, Ben Van Ommen, TNO, Netherlands Claudia Mazzà, Univ Sheffield, Alexander Tuchel Tuchel, Medisana, Germany Massimo Bernaschi, CNR, Italy Clare Samson, Consiglio Nazionale delle Ricerchi, Italy Teresa Colombo, Consiglio Nazionale delle Ricerchi, Italy Gastone Castellani, Università di Bologna, Italy Miriam Capri, Università di Bologna, Italy Paolo Garagnani, Università di Bologna, Italy Stefano Salvioli, Università di Bologna, Italy Viet Anh Nguyen, University of Cambridge, Ivana Bobeldijk-Pastorova, TNO, Netherlands Shaji Krishnan, TNO, Netherlands Aurelio Cappozzo, Università di Roma Foro Italico, Italy Massimo Sacchetti, Università di Roma Foro Italico, Italy Micaela Morettini, Università di Roma Foro Italico, Italy Marc Ernst, Medisana, Germany |
Short Abstract: MISSION-T2D aims to pave the way for translating multilevel immune-metabolic models into the clinical setting of type 2 diabetes. This approach will generate predictive biomarkers from the integration of clinical data with metabolic, nutritional, immunological, genetic and microbiota profiles. It should prove possible to translate these into mobile-based diagnostic tools. |
Poster - Q25 |
Differences between annotations from RBP motif occurrences and CLIP-seq clusters |
Paula Reyes, Universidad Antonio Nariño, Colombia |
Brenda Aguacia-Benitez, Universidad Antonio Nariño, Colombia Cesar Speck-Hernandez, Universidad Antonio Nariño, Colombia Carlos Sierra, Universidad Antonio Nariño, Colombia |
Short Abstract: In this study, we compared the annotations from RBP motif occurrences on the genome and annotations from motif occurrences on CLIP-seq clusters, and we found notable differences that suggest sequence motif is not enough to predict the regions where the RBP binds. |
Poster - Q26 |
Evolution of virulence and drug resistance in Pseudomonas aeruginosa LESB58 |
Rajeev Azad, University of North Texas, United States |
Short Abstract: Liverpool epidemic strain of Pseudomonas aeruginosa is an opportunistic pathogen implicated in cystic fibrosis. This strain, namely, LESB58, is known to have a propensity to acquire virulence associated and antibiotic resistance genes through the process of horizontal gene transfer. Often these genes arrive in large clusters, referred to as “genomic islands”. Horizontal transfers of genomic islands harboring virulence and antibiotic resistance genes have spawned many new virulent and antibiotic resistant strains. In order to decipher the evolution of pathogenicity and resistance in the highly resistant and aggressive bacterial strain LESB58, we implemented a recursive segmentation and agglomerative clustering procedure based on Jensen-Shannon entropic divergence to delineate large regions with atypical composition. Because genomic islands are often mosaic, we also leveraged the ability of our integrative methodology in deciphering the mosaic compositional structure of islands in LESB58 strain and in understanding the contribution of mosaicism in pathogenicity. Of the 6062 genes in this strain, we identified 606 genes residing on 22 predicted genomic islands. We further performed sequence alignment to identify potential donor strains. Most donor strains were opportunistic virulent pathogens implicated in cystic fibrosis. Horizontal transfers of genes among these virulent and antibiotic resistant microorganisms living within cystic fibrosis patients have led to a more morbid and multi-drug resistant LESB58 strain. We have also found several previously unidentified genomic islands in LESB58. These newly found islands, harboring many pathogenicity associated genes revealed by sequence comparisons, have likely made LESB58 strain hypervirulent and mutidrug resistant. |
Poster - Q27 |
Isohemigossypolone as inhibitor of metalloprotease from Bothrops pauloensis: An approach for molecular docking and molecular dynamics. |
Ricardo Gonçalves, Universidade Federal de Goías, Brazil |
Mirian Mendes, Universidade Federal de Goias, Brazil Sâmela Vieira, Universidade Federal de Uberlândia, Brazil Roosevelt da Silva, Universidade Federal de Goias, Brazil |
Short Abstract: The compound is a isohemigossypolone naphthoquinone extracted from the bark of Pachira aquatica, was known as an excellent antifungal, however in our studies was used for neutralization of Bothrops pauloensis In this study, through simulations of molecular docking, we have checked the modes of interaction between isohemigossypolone and metalloprotease. |
Poster - Q28 |
In Silico analysis of the model archeon Halobacterium salinarum anti-sense transcriptome |
Ricardo Vencio, Universidade de Sao Paulo, Brazil |
Livia Zaramela, Universidade de Sao Paulo, Brazil Felipe ten Caten, Universidade de Sao Paulo, Brazil Diego Salvanha, Universidade de Sao Paulo, Brazil Tie Koide, Universidade de Sao Paulo, Brazil |
Short Abstract: None On File |
Poster - Q29 |
Whole-genome analysis of Mannheimia haemolytica serotype A2 to identify potential vaccine candidates against acute pneumonia |
Eduardo Juscamayta, UNMSM, Peru |
Lenin Maturrano University of San Marcos, Peru Eduardo Juscamayta, UNMSM, Peru |
Short Abstract: Mannheimia haemolytica is considered one of the etiological agent of acute pneumonia in cattle and sheep and it has been associated with pneumonia in young alpacas, limiting their productivity. The availability of the genome sequence of M. haemolytica has allowed us to identify potential vaccine candidates. |
Posters
Poster Presentation List & Schedule
Odd numbers:
Poster set up: Day 1 - all day long
Take down: Day 2 after Poster Session
Size: Up to 90cm width x 120 cm height
Even Numbers:
Poster set up: Day 2 after Poster session and Day 3 until the first coffee break
Take Down: Day 3 after Poster Session
Size: Up to 90cm width x 120 cm height
View Posters By Category |
- A) Bioinformatics of Disease and Treatment
- B) Bioinformatic tools and databases
- C) Computational aspects
- D) Comparative Genomics
- E) Education
- F) Epigenetics
- G) Functional Genomics
- H) Genome Organization and Annotation
- I) Genetic Variation Analysis
- J) Metagenomics
- K) Pathogen informatics
- L) Population Genetics Variation and Evolution
- M) Protein Structure and Function Prediction and Analysis
- N) Proteomics
- O) Sequence Analysis
- P) Systems Biology and Networks
- Q) Other
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