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- RNA-seq
- RNA-Seq5
- Bioinformatics4
- Galaxy4
- Transcriptomics4
- bioinformatics4
- Gene Expression3
- RNA-Seq2
- ChIP-seq2
- HDRUK2
- NGS2
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- R-programming1
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Scientific topic
- WTSS
- Bioinformatics4
- MicroRNA sequencing4
- RNA sequencing4
- RNA-Seq4
- RNA-Seq analysis4
- Small RNA sequencing4
- Small RNA-Seq4
- Small-Seq4
- Transcriptome profiling4
- Whole transcriptome shotgun sequencing4
- miRNA-seq4
- ChIP-exo2
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- Chip Seq2
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- Codon usage1
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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
- Analysis1
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Exome variant detection1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
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- Workshops and courses4
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- France2
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Organizer
- ABiMS (http://abims.sb-roscoff.fr/), AVIESAN (http://www.aviesan.fr/en), BiGEst (http://bigest.unistra.fr/), IFB (https://www.france-bioinformatique.fr/), IFB Core (https://www.france-bioinformatique.fr/), MIGALE (https://migale.inrae.fr)1
- Australian BioCommons1
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