LIST OF ACCEPTED RECOMB 2012 PAPERS FOR POSTERS

 

SATURDAY & SUNDAY POSTER SESSIONS ORDER (download).

Download this list of accepted posters in pdf here.

  • Hatice Osmanbeyoglu and Xinghua Lu. Investigating Mechanisms of Estrogen-Mediated Repression of ERα Target Genes in Breast Cancer Cell Lines
  • Sean Chun-Chang Chen, Feng-Chi Chen and Wen-Hsiung Li. Distinct evolutionary rates of phosphorylated and nonphosphoryalted amino acid residues in mammals
  • David Sankoff, Chunfang Zheng and Baoyong Wang. A model for biased fractionation after whole genome duplication
  • Ana Paula Leite, Maxim N. Artyomov, Fadi Towfic and Aviv Regev. Systematic identification of topologically essential interactions in regulatory networks
  • David Knox and Robin Dowell. Automated Generation of Stochastic Model Rules for Single Cell Simulation of Transcriptional Regulation Mechanisms
  • Serghei Mangul, Adrian Caciula, Nicholas Mancuso, Ion Mandoiu and Alex Zelikovsky. Poster : An Integer Programming Approach to Novel Transcript Reconstruction from Paired-End RNA-Seq Reads
  • Noah Daniels, Raghavendra Hosur, Bonnie Berger and Lenore Cowen. SMURFLite: combining simplified Markov random fields with simulated evolution improves remote homology detection for beta-structural proteins
  • Andre E. Minoche, Juliane C. Dohm and Heinz Himmelbauer. Errors and biases in Illumina second generation sequencing data
  • Eva Maria Novoa, Mariana Pavon-Eternod, Tao Pan and Lluis Ribas de Pouplana. A role for tRNA modifications in genome structure and codon usage
  • Gwo-Yu Chuang, Jeffrey Boyington, Michael Joyce, Jiang Zhu, Gary Nabel, Peter Kwong and Ivelin Georgiev. Bioinformatics Prediction Of N-linked Glycosylation Incorporating Structural Properties and Patterns
  • Chan-Shuo Wu, Chun-Ying Yu, Ching-Yu Chuang, Hung-Chih Kuo and Trees-Juen Chuang. Identification and analysis of trans-splicing in human embryonic stem cells by transcriptome sequencing
  • Sayed Mohammad Ebrahim Sahraeian and Byung-Jun Yoon. NAPAbench: a comprehensive network alignment benchmark
  • Leonid Nazarov, Yan Stirmanov, Sergey Larionov, Sergey Rybalko, Eugene Ryadchenko and Alexander Loskutov. The Nature of Extremophiles Genomes Clusterization by Detrended  Fluctuation Analysis
  • Aida Ouangraoua, Krister Swenson and Anne Bergeron. On the comparison of sets of alternative transcripts
  • Chih-Hung Chang, Hsiang-Iu Wang, Hsiang-Chia Lu, Hong-Hwa Chen, Chuan Yi Tang and Hsin-Hung Yeh. A hierarchical screening strategy for gene functional analysis using RNA interference
  • Oscar Flores and Modesto Orozco. Automatic annotation of nucleosome positions: from peaks to reads
  • Mario Fasold, David Langenberger, Hans Binder, Peter F. Stadler and Steve Hoffmann. DARIO: A ncRNA detection and analysis tool for next-generation sequencing experiments
  • Mahdi Belcaid, Anne Bergeron, Aida Ouangraoua, Philippe Lavoie-Mongrain, Nicolas Massoulier and Guylaine Poisson. Duplications in tape measure proteins
  • Shih-Yi Chao and A-Mei Huang. Metastatic Pathway Identification – a case study of prostate cancer
  • Yan Jing, Ping Han and Xiaofeng Song. Intracellular protein stability correlated with the features of the solvent accessible surface
  • Florian Rasche, Kerstin Scheubert, Franziska Hufsky, Marco Kai, Ales Svatos and Sebastian Böcker. Characterisation of unknown metabolites by tandem mass spectrometry
  • Tobias Rausch, Thomas Zichner, Andreas Schlattl, Adrian Stütz, Vladimir Benes and Jan Korbel. DELLY: Structural variant discovery at single-nucleotide resolution
  • Rocio Rebollido-Rios, Stanislav Jakuschev and Daniel Hoffmann. HOW DOES THE CALCIUM BINDING COULD AFFECT THE SUSPECTED PROTEASE ACTIVITY OF SONIC HEDGEHOG?
  • Nadia El-Mabrouk, Yves Gagnon and Mathieu Blanchette. Ancestral Genome Reconstruction based on Gapped Adjacencies
  • Sangcheol Kim, Seulji Lee, Byungwook Lee, Sanghyuk Lee, Sungwon Kwon and Johan Lim. Stouffer's Test in a Large Scale Simultaneous Hypothesis Testing
  • Lydia Hopp, Henry Wirth, Mario Fasold, Markus Loeffler and Hans Binder. Portraying the expression landscapes of cancer subtypes
  • Krister Swenson and Nadia El-Mabrouk. Correcting Errors in Reconciliation
  • Asif Naqvi, Shaymaa Bahnassy, Kuldeep Uchadia, Rinkesh Goyal, Luccky Sharma and Aruna Devi. Study to test the inhibitory activity of THC- Δ9-tetrahydrocannabinol and its derivatives on Acetylcholinesterase (AChe) enzyme: A Molecular Modeling Study
  • Philippe Serhal and Sébastien Lemieux. Correction of spatial bias in oligonucleotide array data
  • Atsushi Niida, Seiya Imoto, Teppei Shimamura and Satoru Miyano. Statistical model-based testing for identification of recurrent genomic aberrations
  • Byungwook Lee. Quantification of transcriptome from RNA-Seq data by effective length normalization
  • Matthias Scholz. A missing data approach to validate nonlinear PCA
  • Çiğdem Sevim Bayrak and Burak Erman. Predicting the Most Probable Conformations of a Given Peptide Sequence in the Random Coil State
  • Thibaut Hourlier, Daniel Barrell, Susan Fairley, Magali Ruffier, Carlos Garcia Giron, Rishi Nag, Simon White, Andreas Kähäri, Amonida Zadissa, Bronwen Aken, Stephen Searle and Tim Hubbard. Ensembl and RNA-Seq: towards better genome annotation!
  • Melanie Schirmer, Christopher Quince, William T. Sloan and David Taylor. Benchmarking of Viral Haplotype Reconstruction Programs
  • H.M.Mahadeva Swamy, Ramasamy Asokan and Riaz Mahmood. Bacillus thuringiensis Cry1I and Cry3A Coleopteran-active insecticidal crystal Proteins: Homology-based 3D Modelling and Implications for Toxin Activity
  • Rahul Agarwal, Matthew Kent, Eli Grindflek, Maren Van Son and Sigbjørn Lien. Whole-Genome Resequencing Identifies Variants Within QTL Regions for Boar Taint
  • Kwang Su Jung and Kiejung Park. An aCGH-based Tool for Detecting Genomic Variation
  • Reshmi G, Sona Charles and Radhakrishna .M Pillai. Systems-Level Dynamical Network Modeling for Identifying Interactomes of Innate Immune Pathways in Dengue Hemorrhagic Fever
  • Mar Gonzàlez-Porta, Miquel Calvo, Michael Sammeth and Roderic Guigó. Estimation of alternative splicing variability in human populations
  • Marie Trussart, Davide Bau, Marc A. Marti-Renom, Eva Yus Najera and Luis Serrano Pubul. The three-dimensional genome conformation of Mycoplasma pneumoniae
  • Ionas Erb, Juan Ramon González-Vallinas, Giovanni Bussotti, Enrique Blanco, Eduardo Eyras and Notredame Cedric. Use of ChiP-Seq data for the design of a multiple promoter-alignment method
  • Joao Curado, Hagen Tilgner and Roderic Guigo. Modeling splicing from chromatin
  • Juliane C. Dohm, Andre E. Minoche, Daniela Holtgraewe, Thomas Rosleff Sörensen, Richard Reinhardt, Hans Lehrach, Bernd Weisshaar and Heinz Himmelbauer. Drafting a large genome at high quality: Multi-platform sequence assembly and integration with genetic and physical maps of sugar beet (Beta vulgaris)
  • Sumeet Dua and Afolabi Olomola. Functional Model Discovery from Gene Expression Time Series using Markov Models
  • Fernando Meyer, Stefan Kurtz and Michael Beckstette. Fast and flexible approximate database search for RNA sequence-structure patterns
  • Md Jamiul Jahid and Jianhua Ruan. A randomized Steiner-tree approach for biomarker discovery and classification for breast cancer metastasis
  • Ines de Santiago, Tom Carroll and Ana Pombo. SeqGI: Sequence Read Enrichment at Genomic Intervals
  • Danielle Hyun-Jin Choi and Brett Tyler. Mathematical Modeling of Phytophthora sojae Effector Gene Evolution
  • Youn-Jae Kim, Jong-Eun Lee, Heon Yoo, Seung-Hoon Lee and Jong Bae Park. Lung cancer brain metastasis-specific mutations identified by exome sequencing  
  • Yuri Pritykin and Mona Singh. Confirmation of Date and Party Hubs across Organisms
  • Seung Gu Park and Sun Shim Choi. Evolutionary non-random flow of synonymous codon usage in multiple organisms
  • Jae Yong Nam, Seung Gu Park and Sun Shim Choi. Analysis of evolutionary characteristics of protein secondary structural units
  • Biter Bilen and Mihaela Zavolan. Probabilistic framework to identify crosslinked positions in RNA-binding protein crosslinking and immune-precipitation data
  • José Ignacio Lucas Lledó and Mario Cáceres. Detection of chromosomal inversions with paired-end sequencing
  • Jascha Casadio, Oriol Fornés, Elena Hidalgo, José Ayté, Isabel Calvo Arnedo, Patricia Garcia and Baldo Oliva. A computational analysis of the regulation of oxidative stress genes in S. pombe by Pap1 and Prr1
  • Nikita Alexeev. Random matrix approach and Combinatorial topology approach to Sorting by transpositions
  • Fahad Syed, Mikko Arvas, Marja Ilmen and Tiina Nakari-Setala. Comparison of Bacterial Genomes
  • Thomas Bonfert, Gergely Csaba, Ralf Zimmer and Caroline C. Friedel. A context-based approach to identify the most likely mapping for RNA-seq experiments
  • Santi González, Bàrbara Montserrat-Sentís, Friman Sánchez, Montserrat Puiggròs, Enrique Blanco, Laura Martinez, Alex Ramirez and David Torrents. Prediction of regulatory regions using ReLA
  • Daeyong Jin and Hyunju Lee. A computational approach to identifying gene-microRNA regulatory modules in cancer
  • Tomasz Arodz and Przemyslaw Plonka. Uncovering the Distribution of Protein Structure Change Magnitudes upon Single Amino Acid Substitutions
  • Oznur Tastan, Yanjun Qi, Jaime G. Carbonell and Judith Klein-Seetharaman. Refining Literature Curated HIV-1, Human Protein-Protein Interactions Using Expert Opinions
  • Juan González-Vallinas and Eduardo Eyras. Predicting and characterizing active enhancers in cancer using high-throughput sequencing data
  • Arnald Alonso, Sara Marsal and Antonio Julià. CNStream2: a fast and highly accurate tool for SNP and CNV genotyping with Illumina microarrays
  • Jairo Rocha and Ricardo Alberich. The Significance of the ProtDeform Score for Structure Prediction and Alignment
  • Sonja Althammer, Amadis Pages and Eduardo Eyras. Models of regulatory genomics
  • Ole Schulz-Trieglaff, Elizabeth Murchison, Zemin Ning and Anthony Cox. The devil is in the detail: mining and annotating genomic variants in the Tasmanian Devil facial tumour genome
  • Paweł P. Łabaj and David P. Kreil. Improving RNA-Seq precision with MapAl
  • Tobias Marschall, Ivan Gesteira Costa, Stefan Canzar, Markus Bauer, Gunnar W. Klau, Alexander Schliep and Alexander Schoenhuth. CLEVER: Clique-Enumerating Variant Finder
  • Sílvia Bonàs, Josep M. Mercader and David Torrents. Empirical evaluation of different modern reference panels for imputation and their implication for Genome Wide Association Studies.
  • Hayan Lee and Michael Schatz. Genomic Dark Matter: The reliability of short read mapping illustrated by the Genome Mappability Score
  • Boris Fedorov, Leonid Zaslavsky, Vyacheslav Chetvernin, Stacy Ciufo, Boris Kiryutin, Kathleeen O'Neill, Alexandre Souvorov, Igor Tolstoy and Tatiana Tatusova. Integrated system for bacterial pan-genome analysis
  • Miler Lee, Ariel Bazzini, Polloneal Ocbina, Carter Takacs and Antonio Giraldez. Computational analysis of ribosome profiling data to characterize translational dynamics in Zebrafish
  • Itrat Fatima and Shaneen Singh. Computational Analysis of GRAM domains in the model plant Arabidopsis thaliana.
  • Irina Khrebtukova, Ryan Kelley, Shujun Luo, Tim Hill, Patrick Lau, Jennifer Chiniquy, Kathryn Stephens, Semyon Kruglyak and Gary P Schroth. Automated workflow for RNA-Seq analysis: application and testing with various types of RNA-Seq protocols
  • Jennifer Fang, Siddarth Selvaraj, Jesse Dixon, Feng Yue, Ming Hu, Ke Deng, Zhaohui Qin, Yixin Zhu, Jun Liu and Bing Ren. 3D Chromosome Structure Visualization from Hi-C Data
  • Orion Buske, Ashokkumar Manickaraj, Seema Mital and Michael Brudno. Identification of deleterious synonymous variants in human genomes
  • James Morton, Patricia Abrudan, Chun Liang and John Karro. Tools for Cleaning NGS Transciptome Data
  • Andreas Untergasser, Ioana Cutcutache, Triinu Koressaar, Jian Ye, Brant C. Faircloth, Maido Remm and Steve Rozen. Primer3 - New Capabilities and Interfaces
  • Jeeyoung Shin, Minkyu Shin and Yangseok Kim. Association Investigator: The intelligent for investigating the relationship between genomics data and clinical variables
  • Ray Marin and Jiri Vanicek. PACCMIT: Prediction of ACcessible and/or Conserved MIcroRNA Targets
  • Marta Mele, Roderic Guigó and Tomàs Marquès. Studying lncRNAs in great ape evolution
  • Merja Oja, Paula Jouhten, Eija Rintala, Mervi Toivari, Marilyn Wiebe, Laura Ruohonen and Merja Penttilä. Systems biology for studying the physiology of acid producing yeast
  • Jeongkyun Kim, Hee-Jin Lee, Jong C. Park and Hyunju Lee. A search engine for recommending cancer-related genes based on literature evidence
  • Catarina Allegue, Óscar Campuzano, Lucía Quintana, Carles Ferrer, Sergio Castillo, Eduardo Salas, Mónica Bayés, Simon Heath, Anna María Iglesias, Mónica Coll and Ramon Brugada. VALIDATION OF A NGS STRATEGY FOR GENETIC SCREENING OF SUDDEN CARDIAC DEATH
  • Panagiotis Papasaikas and Juan Valcarcel. Multiple Links between Splicing Regulation and Chromatin Revealed by an Integrated Analysis of High-throughput Chromatin and Splicing Perturbation Data.
  • Juan Ramon Tejedor, Panagiotis Papasaikas and Juan Valcarcel. Reconstruction of a Splicing Regulatory Circuitry Involved in Cell Proliferation and Apoptosis.
  • John R. .Mcpherson, Yingting Wu, Patrick Tan and Steve Rozen. Identifying Genomic Copy Number Alteration and Loss of Heterozygosity in Next-Generation Sequence Data
  • Teppei Shimamura, Seiya Imoto, Atsushi Niida and Satoru Miyano. Identification of key methylated genes from patient-specific gene networks
  • Agata Wesołowska, Louise Borst, Marlene Dalgaard, Louise Helt, Hans Madsen, Hanne Marquart, Peder Wehner, Morten Rasmussen, Eske Willerslev, Thomas Gilbert, Søren Brunak, Kjeld Schmiegelow and Ramneek Gupta. Relating genomic variation to drug response in childhood acute lymphoblastic leukemia
  • Baeksoo Kim and Hyunju Lee. A cancer text ranking algorithm based on cancer-related terms
  • Andreas Leha, Tim Beißbarth and Klaus Jung. Predicting Ordinal Response in High-Dimensional Datasets
  • Nikolay Chekanov, Egor Prokhortchouk, Artem Artemov, Artem Nedoluzhko, Eugenia Bulygina, Sergey Rastorguev, Svetlana Tsygankova, Natalia Gruzdeva and Konstantin Skryabin. A family study of early-onset Alzheimer's disease
  • Sònia Casillas, Can Alkan, Evan E Eichler and Mario Cáceres. Calling inversions from Next-Generation Sequencing Paired-End Mapping data with GRIAL
  • Evrim Besray Unal, Maria Lluch, Eva Yus, Yogi Jaeger and Luis Serrano. Reverse Engineering of Mycoplasma pneumoniae Gene Regulatory Network
  • Paweł Bednarz, Agnieszka Podsiadło, Joanna Giemza, Norbert Dojer and Bartek Wilczynski. BNFinder2: efficient software for learning Bayesian networks
  • Cemal Erdem, Alper Demir, Ahmet Gül and Burak Erman. Mathematical Modeling of a Human Immune-Mediated Auto-Inflammatory Disease
  • Ian Streeter, David Thybert, Klara Stefflova, Laura Clarke, Duncan Odom and Paul Flicek. A comparison of read-mapping and de novo assembly methods for calling inter-species variants between Mus caroli and Mus musculus
  • Prerna Dua, Chaitanya Pinnamaneni, Pradeep Chowriappa and Walter Lukiw. A Co-expression Network Based Approach for Gene Expression Analysis in Alzheimer’s’ Disease Progression
  • Alexander Martinez Fundichely, Meritxell Oliva Pavia, Juan Ramon Gonzalez Ruiz, Sònia Casillas and Mario Cáceres. Accurate prediction of inversions in the human genome from paired-end mapping data with the GRIAL algorithm.
  • Layla Oesper, Anna Ritz, Sarah Aerni, Ryan Drebin and Ben Raphael. Reconstructing Cancer Genomes from Paired-end Sequencing Data
  • Maike Ahrens, Jörg Rahnenführer, Christian Stephan and Martin Eisenacher. Detecting features from OMICS data that contain subgroups of patients with differential values
  • Sinan Erten, Salim A. Chowdhury, Xiaowei Guan, Rod K. Nibbe, Jill S. Barnholtz-Sloan, Mark R. Chance and Mehmet Koyuturk. Identifying stage-specific protein subnetworks for colorectal cancer
  • Derya Aydın, Meltem Muftuoglu and Burak Erman. Identifying small molecule inhibitors targeting base excision repair enzymes DNA polymerase γ and β to increase the effects of cancer treatment
  • Rachita Yadav, Klaus Bønnelykke, Thomas Nordahl Petersen, Anne Mølgaard, Hans Bisgaard and Ramneek Gupta. Machine learning risk prediction of childhood asthma.
  • David Dufour and Marc A. Marti-Renom. RNA structure prediction by knowledge-based statistical potentials and Selective 2′-Hydroxyl Acylation and Primer Extension (SHAPE)
  • Susanne Balzer, Ketil Malde, Markus A. Grohme and Inge Jonassen. Filtering duplicate reads from 454 pyrosequencing data
  • Oliver Drechsel, Rubayte Rahman and Stephan Ossowski. Clinical application and computational analyses of Exome-seq for disease studies
  • Kalliopi Tsafou, Damian Plichta, Branka Radić, Uwe Rix, Giulio Superti-Furga, Irene Kouskoumvekaki and Ramneek Gupta. Investigating the Genomic Landscape of Ewing Sarcoma
  • Matthew Ruffalo, Mehmet Koyuturk, Soumya Ray and Thomas Laframboise. Accurate Estimation of Short Read Mapping Quality for Second-Generation Genome Sequencing
  • Jon Hallander, Petter Lindgren, Pär Larsson and Andreas Sjödin. A microbial forensic approach using Ultra-Deep Sequencing (UDS) for analysis of haplotype spectra in clonal bacterial strains
  • Yuichi Shiraishi, Yusuke Sato, Aiko Sato-Otsubo, Yusuke Okuno, Shigekatsu Maekawa, Hidewaki Nakagawa, Seishi Ogawa and Satoru Miyano. Fusion gene detection by using soft clipping information
  • Juris Viksna, Karlis Freivalds and Paulis Kikusts. Application of graph clustering and visualization methods for detection of evolutionary related groups of proteins
  • Chiara Fornari, Francesca Cordero, Marco Beccuti, Stefania Lanzardo, Laura Conti, Federica Cavallo, Gianfranco Balbo and Raffaele Calogero. Multi-level model for the investigation of oncoantigen-driven vaccination effect
  • Marc Friedländer, Esther Lizano, Eulàlia Martí and Xavier Estivill. NATA: a combined wetlab and drylab method for naïve transcriptome analysis
  • Oriol Fornes and Baldo Oliva. Prediction of DNA-binding specificities using statistical potentials
  • Eva König, Lars Feuerbach, Barbara Hutter, Matthias Schlesner, Qi Wang, Benedikt Brors and Thomas Lengauer. Improving loss of  heterozygosity identification by tumor purity estimation
  • Matthew Edwards and David Gifford. High-resolution genetic mapping with pooled sequencing
  • Joseph Herman, Ádám Novák, Rune Lyngsø and Jotun Hein. A probabilistic framework for incorporating alignment uncertainty into multiple sequence analysis
  • Abhishek Mitra and Maga Rowicka. Instant-Seq:- an integrated tool with web interface for fast analysis of ChIP-Seq data
  • Dhany Saputra, Thomas Sicheritz Pontén and Ole Lund. Reads2Type: An Online Tool for Rapid Bacterial Typing
  • Sana Ben Mustapha, Hend Ben Tamarzizst, Ghada Baraket and Amel Salhi Hannachi. SSR markers and sequences of the trnL intron to study polymorphism in Tunisian plum            
  • Ornella Cominetti, David Smith, Nick Jones, Radek Erban, Philip Maini and Climent Casals-Pascual. Identification of new pathobiological clusters in severe malaria using unsupervised methods
  • Anna Ritz, Suzanne Sindi, Ali Bashir and Benjamin Raphael. A Probabilistic Method for Structural Variant Prediction from Strobe Sequencing Data
  • Anne Wenzel, Erdinc Akbasli and Jan Gorodkin. RIsearch: fast yet accurate RNA-RNA interaction search
  • Fabio Vandin, Hsin-Ta Wu, Eli Upfal and Ben Raphael. Algorithms to Find Mutated Pathways in Cancer
  • Jon Sveinbjornsson and Bjarni Halldorsson. BAM Region Viewer: A Viewer Application For BAM
  • Sonia Boughattas. SNPs identification, multiple alignment and network construction to analyze the polymorphism of Tunisian strains of the parasite Toxoplasma gondii
  • Maga Rowicka, Nicola Crosetto, Abhishek Mitra, Maria Joao Silva, Magda Bienko, Philippe Pasero and Ivan Dikic. BLESS: mapping DNA double-strand breaks by next-generation sequencing
  • Myungguen Chung and Kie-Jung Park. Automated analysis support system for Imputed Genotype based Case-Control Study with a Disease by using next-generation sequencing data
  • Nathan Boley. Integrative De Novo Transcriptome Assembly in Fruit Fly
  • Manway Liu, Anupama Reddy, Alan Huang, Giordano Caponigro and Joseph Lehar. Network Analysis of Pharmacologic, Genomic, and Transcriptomic Assays in Cancer Cell Lines
  • Alejandro Caceres, Suzanne Sindi, Benjamin Raphael, Mario Caceres and Juan Gonzalez. Identification of Polymorphic Inversions from Genotypes
  • Jin Zhang, Jiayin Wang and Yufeng Wu. Calling Structural Variations with Low-coverage Sequencing Data by Mapping to Focal Region
  • Jeanre Smit, Misha Le Grange, Phelelani Mpangase, Michal Szolkiewicz and Fourie Joubert. Discovery: a resource for the rational selection of drug target proteins and leads for the malaria parasite, Plasmodium falciparum

 

CALL FOR POSTERS RECOMB 2012

RECOMB 2012 invites the submissions of abstracts for the Posters track. Deadline: 1 March 2012.

Please submit a one-page abstract (about 200 words, plain justified text in at least 10pt character size, formatted to fit European Standard A4: 21 x 29.7 cm) of your Poster including title, author(s), affiliation, e-mail and abstract text, to the http://www.easychair.org/conferences/?conf=recomb2012.

Accepted posters will be published on this website on 8th March. The actual poster space will be 90 x 120 cm (width x height), which corresponds to A0 VERTICAL format (or 16 pages in A4 format). The accepted poster abstracts will be published in the conference book of abstracts. In addition, one poster will be chosen for awards.

 

EXTEND THE LIFE OF YOUR POSTER

We invite all RECOMB2012 poster presenters to deposit the recently presented poster/presentation(s) at RECOMB2012 in the established open access poster repository. If you would like to do so, then just go to http://f1000.com/posters/depositor. A few of you have already deposited their posters; http://f1000.com/posters/browse?conferenceId=86444301.

A further list of the most commonly asked questions, with answers, can be found here (http://f1000.com/posters/fordepositors). 

The posters thus far have proved very popular with our large base of Anesthesiology users, and deposition of your work can help extend the visibility, and maximize your work’s value by dramatically increasing access and enabling others to benefit from new research.

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RECOMB 2012 in cooperation with Faculty of 1000 invites poster presenters at this year’s meeting to deposit their poster and presentation slides(s) following the meeting into the established open access poster repository, F1000 Posters, to enable those who could not make the meeting see the novel work on display. F1000’s expert Faculty of ~10,000 members will then view these submissions to identify those they wish to select for positive evaluation in the award winning F1000 post-publication peer review service.