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Issue |
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Vol 21: Supplement A |
COST Action BM1006 (SeqAhead) closing conference "Next Generation Sequencing: a look into the future” |
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Lubos Klucar, Teresa K. Attwood, Erik Bongcam-Rudloff |
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Vol 17: Supplement B |
A combinatorial and integrated method to analyse RNA-seq reads |
Abstract
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Nicolas Philippe, Mikael Salson, Therese Commes, Eric Rivals |
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Vol 17: Supplement B |
Bioinformatics developments for NGS data analysis at PRABI |
Abstract
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Franck Picard, Guy Perrière |
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Vol 17, No 1: Next Generation Sequencing Data Analysis |
SEQAHEAD - COST Action BM1006: Next Generation Sequencing Data Analysis Network |
Abstract
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Teresa Attwood, Erik Bongcam-Rudloff, Andreas Gisel |
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Vol 17: Supplement B |
RSAT peak-motifs: fast extraction of transcription factor binding motifs from full-size ChIP-seq datasets |
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Morgane Thomas-Chollier, Matthieu Defrance, Olivier Sand, Carl Herrmann, Denis Thieffry, Jacques van Helden |
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Vol 17: Supplement B |
The Vital-IT HPC and the Swiss-Prot group |
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Laurent Falquet |
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Vol 17: Supplement B |
The Norwegian Sequencing Centre (NSC) |
Abstract
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Robert Lyle, Tim Hughes, Dag Undlien, Kjetill Jakobsen |
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Vol 17: Supplement B |
Exploration of environmental metagenomes and metatranscriptomes: current possibilities and limitations in data analysis |
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Petr Baldrian |
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Vol 17: Supplement B |
BioinformaticsTools@bioacademy.gr |
Abstract
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Athanasia Pavlopoulou, Sophia Kossida |
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Vol 17: Supplement B |
Statistical approaches for the analysis of RNA-Seq and ChIP-seq data and their integration |
Abstract
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Claudia Angelini, Italia De Feis |
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Vol 17: Supplement B |
smallRNA data analysis |
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Angelica Tulipano, Andreas Gisel |
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Vol 17: Supplement B |
Digital gene expression data, cross-species conservation and noncoding RNA |
Abstract
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Nicolas Philippe, Florence Ruffle, Elias Bou-Samra, Anthony Boureux, Thérèse Commes, Eric Rivals |
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Vol 17: Supplement B |
TAPYR: An efficient high-throughput sequence aligner for re-sequencing applications |
Abstract
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Francisco Fernandes, Paulo G.S. da Fonseca, Luis M.S. Russo, Arlindo L. Oliveira, Ana T. Freitas |
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Vol 17: Supplement B |
The Seal suite of distributed software for high-throughput sequencing |
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Luca Pireddu, Simone Leo, Gianluigi Zanetti |
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Vol 17: Supplement B |
Epigenomic and transcriptional effects of Dnmt3b mutations in human ICF syndrome-derived B cell lines. |
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Sole Gatto, Claudia Angelini, Sylwia Leppert, Valentina Proserpio, Sarah Teichmann, Maurizio D’Esposito, Maria R. Matarazzo |
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Vol 17: Supplement B |
UPPNEX - A solution for Next Generation Sequencing data management and analysis |
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Samuel Lampa, Jonas Hagberg, Ola Spjuth |
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Vol 17: Supplement B |
EU COST Action TD0801: Statistical Challenges On The 1000 Euro Genome Sequences In Plants |
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Marco C.A.M. Bink, Thomas Schiex |
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Vol 17: Supplement B |
Read indexing |
Abstract
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Nicolas Philippe, Mikael Salson, Thierry Lecroq, Martine Leonard, Therese Commes, Eric Rivals |
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Vol 17: Supplement B |
From cutadapt to sequencetools (sqt): a versatile toolset for sequencing projects |
Abstract
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Marcel Martin, Sven Rahmann |
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Vol 17: Supplement B |
Linking research data with scholarly publications |
Abstract
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Teresa K Attwood, Philip McDermott, James Marsh, Steve R Pettifer, David Thorne |
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Vol 17: Supplement B |
Improved analysis of fungal communities using the next-generation-sequencing analysis of rpb2 genes |
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Tomas Vetrovsky, Jana Voriskova, Lucia Zifcakova, Michaela Urbanova, Petr Baldrian |
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Vol 17: Supplement B |
In the Shadow of the Genome: A Challenging Journey to Diversity in Leishmania donovani |
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Hideo Imamura, An Mannaert, Tim Downing, Matthew Berriman, Jean-Claude Dujardin |
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Vol 17: Supplement B |
NGS data analysis: the user POV |
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Jose R. Valverde, Jose M. Rodríguez, Alexandro Rodriguez-Rojas, Alejandro Couce, Jesus Blazquez |
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Vol 17: Supplement B |
COST Action BM 1006 (SeqAhead): MC BUSINESS MEETING AND SCIENTIFIC MEETING |
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Andreas Gisel, Teresa Attwood, Jacques van Helden, Jose R Valverde, Ana Conesa, Ralf Herwig, Eija Korpelainen, Veli Mäkinen, Steve Pettifer, Alberto Policriti, Thomas Svensson, Gert Vriend, Erik Bongcam-Rudloff |
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Vol 17: Supplement B |
IT Future of Medicine: Next Generation Sequencing is the Key to Future Personalized Medicine |
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Hans Lehrach, Babette Regierer |
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