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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, No 1: Next Generation Sequencing Data Analysis |
SEQAHEAD - COST Action BM1006: Next Generation Sequencing Data Analysis Network |
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Teresa Attwood, Erik Bongcam-Rudloff, Andreas Gisel |
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Vol 17: Supplement B |
Bioinformatics developments for NGS data analysis at PRABI |
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Franck Picard, Guy Perrière |
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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 |
Abstract
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Laurent Falquet |
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Vol 17: Supplement B |
The Norwegian Sequencing Centre (NSC) |
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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 |
Algorithm for error detection in metagonomics NGS data |
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Dimitar Vassilev, Milko Krachunov, Ivan Popov, Elena Todorovska, Valeria Simeonova, Pawel Szczesny, Pawel Siedlecki, Urszula Zelenkiewicz |
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Vol 17: Supplement B |
Massive-scale RNA-Seq experiments in human genetic diseases |
Abstract
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Valerio Costa, Marianna Aprile, Roberta Esposito, Maria Rosaria Ambrosio, Margherita Scarpato, Carmela Ziviello, Italia De Feis, Claudia Angelini, Alfredo Ciccodicola |
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Vol 17: Supplement B |
Innovation and Trends with In-Memory Technology |
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Matthias Steinbrecher |
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Vol 17: Supplement B |
An Integrated RNA-seq Atlas of the Murine T-Helper Cell Transcriptome |
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Andrew Deonarine |
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Vol 17: Supplement B |
Oncogenomics of the Hormone-responsive Breast Cancer Phenotype by NGS |
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Alessandro Weisz |
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Vol 17: Supplement B |
NOIseq: a RNA-seq differential expression method robust for sequencing depth biases |
Abstract
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Sonia Tarazona, Fernando García, Alberto Ferrer, Joaquín Dopazo, Ana Conesa |
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Vol 17: Supplement B |
bcbio-nextgen: Automated, distributed next-gen sequencing pipeline |
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Roman Valls Guimera |
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Vol 17: Supplement B |
Power and limits of capture‐based, targeted DNA resequencing for mutation detection |
Abstract
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Fabrice Lopez, Hélène Holota, François-Xavier Théodule, Jean Imbert |
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Vol 17: Supplement B |
BioinformaticsTools@bioacademy.gr |
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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 |
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Claudia Angelini, Italia De Feis |
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Vol 17: Supplement B |
smallRNA data analysis |
Abstract
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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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