- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Keyword
- RNA-seq
- ISCB16
- OtherEvents13
- EeLP10
- HDRUK10
- eLearning10
- training7
- Computer science4
- life sciences4
- Biotechnology3
- genomics3
- Bioinformatics2
- ChIP-seq2
- ClinicalPharmacology2
- Diseases2
- HPC2
- ISCBEvents2
- Oncology2
- Single Cell Genomics2
- Toxicology2
- Variant detection2
- Workflows2
- bioinformatics2
- next-generation sequencing2
- R-programming1
- Artificial Intelligence1
- BioBB1
- Biomarker Conference1
- Biomarker Conference 20171
- Biomarkers Conference 20171
- Biomarkers Conferences1
- Biomarkers Conferences USA1
- Biomarkers Congress USA1
- Biometrics1
- Biopharmaceuticals1
- CWL1
- Cancer1
- Cloud Computing1
- Computational Biology1
- ComputationalBiology1
- Containers1
- DMP1
- DMP evaluation1
- DMP templates1
- DMP tools1
- Data carpentry1
- Docker1
- EDI1
- EMBnet1
- Evolutinary genomics1
- FAIR Research1
- FAIR principles1
- Genetics1
- Genomics1
- Gynecology1
- Hematology1
- ICSB1
- ISCBCo-SponsoredorAffiliatedEvent1
- Imaging1
- Jupyter notebook1
- MaterialsEngineering1
- Medicine1
- Microarrays1
- Nanotechnology1
- Neurobiology1
- Neurourology1
- Nextflow1
- Open Data1
- Open Science1
- PersonalizedMedicine1
- Pharmacogenomics1
- Population Genomics1
- Precision Medicine1
- Sequence Analysis1
- Software Carpentry1
- Statistics1
- Systems biology1
- Transcriptomics1
- algorithms1
- assembly1
- biomedical applications1
- biomedicine1
- biomolecular simulations1
- clinical genomics1
- comparative genomics1
- competency1
- conda1
- data management1
- data management plan1
- data stewardship1
- design research1
- dimension1
- dynamic simulations1
- equity1
- evaluation1
- galaxy1
- gender1
- high-performance computing1
- inclusion1
- machine learning1
- 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 courses2
- Show N_FILTERS more
-
-
-
Country
- France2
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events