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