- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- NBIS1
- Show N_FILTERS more
-
-
-
Keyword
- next-generation sequencing
- storage
- training22
- ISCB14
- programming12
- reproducibility11
- HDRUK9
- data management9
- data visualisation9
- OtherEvents7
- biostatistics7
- mark ibberson group6
- ISCBCo-SponsoredorAffiliatedEvent5
- open data5
- Oncology3
- basic research3
- data security3
- torsten schwede & thierry sengstag group3
- Biotechnology2
- ChIP-seq2
- DMP2
- Diseases2
- ISCBEvents2
- RNA-seq2
- Single Cell Genomics2
- Variant detection2
- biodiversity2
- bioinformatics2
- christophe dessimoz group2
- comparative genomics2
- evolution and phylogeny2
- evolutionary biology2
- genes and genomes2
- marc robinson-rechavi group2
- non model organisms2
- ontology2
- proteins and proteomes2
- raphael gottardo group2
- robert waterhouse group2
- Bayesianstatistics1
- CWL1
- Chemistry1
- DMP tools1
- Data management plan1
- Docker1
- EeLP1
- FAIR1
- ICSB1
- Reproducibility1
- Workflows1
- alan bridge group1
- data collection1
- data mining1
- data organisation1
- data publication1
- data quality1
- data reuse1
- data sharing1
- data stewardship1
- database curation1
- eLearning1
- experimental biology1
- homology modelling1
- interoperability1
- lifescience1
- machine learning1
- mauro delorenzi & frédéric schütz group1
- mauro delorenzi & frédéric schütz group1
- metadata1
- michael stadler group1
- microscopy1
- modelling and simulation1
- nanotoxicology1
- next generation sequencing1
- olivier michielin & vincent zoete group1
- ontologies, enanomapper1
- protein engineering1
- protein interactions1
- reproduce1
- research data1
- reuse1
- structural biology1
- vincent zoete group1
- Show N_FILTERS more
-
-
-
Scientific topic
- Bioinformatics2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- Chromosome walking2
- Clone verification2
- DNA variation2
- DNA-Seq2
- DNase-Seq2
- De novo genome sequencing2
- Exomes2
- Genetic variation2
- Genome annotation2
- Genome sequencing2
- Genomes2
- Genomic variation2
- Genomics2
- High throughput sequencing2
- High-throughput sequencing2
- MicroRNA sequencing2
- Mutation2
- NGS2
- NGS data analysis2
- Next gen sequencing2
- Next generation sequencing2
- Panels2
- Personal genomics2
- Polymorphism2
- Primer walking2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sanger sequencing2
- Sequencing2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Somatic mutations2
- Synthetic genomics2
- Targeted next-generation sequencing panels2
- Transcriptome profiling2
- Viral genomics2
- WGS2
- WTSS2
- Whole genome resequencing2
- Whole genome sequencing2
- Whole genomes2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Show N_FILTERS more
-
-
-
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
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses3
- Show N_FILTERS more
-
-
-
Country
- France2
- Sweden1
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest3
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events