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Issue |
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Vol 29 |
Ds-Seq: an integrated pipeline for in silico small RNA sequence analysis for host-pathogen interaction studies |
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Temitayo Adebanji Olagunju, Angela Uche Makolo, Andreas Gisel |
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Vol 19: Supplement A |
Next-masigpro: Dealing with RNA-seq time series |
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Ana Conesa, María José Nueda |
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Vol 17: Supplement B |
A combinatorial and integrated method to analyse RNA-seq reads |
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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 |
e-RGA: enhanced Reference Guided Assembly of Complex Genomes |
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Francesco Vezzi, Federica Cattonaro, Alberto Policriti |
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Vol 20 |
Fq_delta - Efficient storage of processed versions of fastq files |
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Andra Veraart, Henk-Jan van den Ham, Maarten A. Bijl, Arno C. Andeweg, Anita C. Schürch |
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Vol 21 |
CexoR: an R/Bioconductor package to uncover high-resolution protein-DNA interactions in ChIP-exo replicates |
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Pedro Madrigal |
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Vol 19: Supplement A |
Comparison of variant calling methods in exome sequencing of matched tumor-normal sample pairs |
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Sara Monzon, Javier Alonso, Gonzalo Gómez, David Gonzalez-Pisano, Isabel Cuesta |
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Vol 19, No 1 |
ICT needs and challenges for Big Data in the Life Sciences. A workshop report - SeqAhead/ISBE Workshop in Pula, Sardinia, Italy, 6 June 2013 |
Abstract
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Babette Regierer, Luca Pireddu, Martijn Moné, Andreas Gisel |
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Vol 19: Supplement A |
High-throughput DNA analysis |
Abstract
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Ivo Gut |
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Vol 19: Supplement A |
Error profiles for Next Generation sequencing technologies |
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Melanie Schirmer, Linda D'Amore, Neil Hall, Christopher Quince |
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Vol 17, No 1: Next Generation Sequencing Data Analysis |
SEQscoring: a tool to facilitate the interpretation of data generated with next generation sequencing technologies |
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Katarina Truvé, Oscar Eriksson, Martin Norling, Maria Wilbe, Evan Mauceli, Kerstin Lindblad-Toh, Erik Bongcam-Rudloff |
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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 18: Supplement A |
Analysis workflow for the identification allelic variants associated with rare disorders using whole genome sequencing approach |
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V Maselli, D Cittaro, E Stupka |
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Vol 20: Supplement A |
NGS data management and analysis for hundreds of projects: Experiences from Sweden |
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Ola Spjuth |
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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 |
The Norwegian Sequencing Centre (NSC) |
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Robert Lyle, Tim Hughes, Dag Undlien, Kjetill Jakobsen |
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Vol 17, No 1: Next Generation Sequencing Data Analysis |
Cutadapt removes adapter sequences from high-throughput sequencing reads |
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Marcel Martin |
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Vol 19: Supplement A |
Automated finished microbial genomes and epigenomes to understand infectious diseases |
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Ralph Vogelsang |
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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 19, No 1 |
EMBnet, the Global Bioinformatics Network, in 2013: A Silver Anniversary |
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Teresa K Attwood |
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Vol 19, No 1 |
2013 Annual General Meeting: Executive Board Report |
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Teresa K Attwood, Andreas Gisel, Etienne de Villiers, Erik Bongcam-Rudloff, Goran Neshich |
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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 19: Supplement A |
Viral Metagenomics – New applications for the broad-range detection of viromes in veterinary and public health settings |
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Oskar Erik Karlsson, Martin Norling, Fredrik Granberg, Sándor Belák, Erik Bongcam-Rudloff |
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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 19: Supplement A |
Automated transcription start site prediction for comparative Transcriptomics using the SuperGenome |
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Alexander Herbig, Cynthia Sharma, Kay Nieselt |
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