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- IFB French Institute of Bioinformatics2
- VIB Conferences1
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Scientific topic
- Genomics
- ChIP-seq
- Exomes3
- Genome annotation3
- Genomes3
- Personal genomics3
- Synthetic genomics3
- Viral genomics3
- Whole genomes3
- Bioinformatics2
- ChIP-exo2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- High throughput sequencing2
- High-throughput sequencing2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- WGS2
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- Whole genome resequencing2
- Whole genome sequencing2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Aerobiology1
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- Targeted proteomics1
- Top-down proteomics1
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Operation
- Consensus-based sequence alignment2
- Constrained sequence alignment2
- Data visualisation2
- Expression analysis2
- Expression data analysis2
- Gene expression analysis2
- Gene expression data analysis2
- Gene expression regulation analysis2
- Genetic variation analysis2
- Genetic variation annotation2
- Metagenomic inference2
- Microarray data analysis2
- Molecular visualisation2
- Multiple sequence alignment (constrained)2
- Oligonucleotide alignment2
- Oligonucleotide alignment construction2
- Oligonucleotide alignment generation2
- Oligonucleotide mapping2
- Peak calling2
- Peak-pair calling2
- Plotting2
- Protein binding peak detection2
- Protein expression analysis2
- Read alignment2
- Read mapping2
- Read pre-processing2
- Rendering2
- Sequence alignment2
- Sequence alignment (constrained)2
- Sequence alignment construction2
- Sequence alignment generation2
- Sequence read pre-processing2
- Sequence variation analysis2
- Short oligonucleotide alignment2
- Short read alignment2
- Short read mapping2
- Short sequence read mapping2
- Transcript variant analysis2
- Variant analysis2
- Visualisation2
- Allele calling1
- Exome variant detection1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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Country
- France2
- Belgium1
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Sponsor
- INSERM
- Lonza
- Aviesan ITMO GGB2
- ELIXIR EXCELERATE2
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- Biorad1
- Centre for Digital Life Norway1
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- ELIXIR Training Platform1
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- EU COST Action G-BiKE1
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- H3ABioNet1
- INRA1
- INTERREG V-A Italy-Slovenia 2014-2020 project T...1
- IRCCS Ospedale San Raffaele1
- InvertOmics1
- LINQ1
- Lexogen1
- Merck1
- NBIS - National Bioinformatics Infrastructure S...1
- NORBIS1
- National Research Council of Italy1
- PANGenS1
- PanACEA1
- SANBI/UWC1
- Swiss Tropical and Public Health Institute1
- The European Union1
- Università Vita-Salute San Raffaele1
- VEIS1
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