- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- BioExcel1
- Show N_FILTERS more
-
-
-
Keyword
- NGS
- Workflows16
- Nextflow8
- Bioinformatics6
- HPC6
- CWL4
- nf-core4
- Galaxy3
- High performance computing3
- bioinformatics3
- workflows3
- Gene expression (gene-expression)2
- HDRUK2
- NCMAS2
- R/Bioconductor2
- Reproducibility2
- Variant-calling1
- Africa1
- Bioinformatics tools1
- Building blocks1
- COBREXA1
- CellNOpt1
- Cloud1
- Cloud computing1
- Computational biology1
- Compute1
- Data analysis1
- Data protection1
- Dbfetch1
- Distributed data analysis1
- Docker1
- Droplet-based single-cell RNA library preparation1
- Expression Atlas1
- FAIR1
- Functional analysis1
- GROMACS1
- GWAS1
- GWAS workflow1
- Gene Expression1
- Genotyping array analysis 1
- Globus1
- H3ABioNet1
- H3ABioNet GWAS 2018 Lecture Series1
- H3Africa genotyping array1
- High Performance Computing1
- Job dispatcher1
- Jupyter notebook1
- KNIME1
- LSF1
- MaBoSS1
- Next generation sequencing data analysis1
- Pathway analysis1
- PhysiBoSS1
- PhysiCell1
- Pipelines1
- Population Genomics1
- Python1
- RNA-seq1
- Reproducible Environment1
- Reproducible Science1
- ReproducibleResearch1
- Research software1
- Scalable Computing1
- SciWorkflows1
- Single cell1
- Snakemake1
- Software engineering1
- Visualization1
- WES1
- WESkit1
- Webinar1
- WorkflowHub1
- computational methods1
- data repository1
- data-analysis1
- digital archives1
- linked data1
- research software1
- scRNA-seq1
- workflUX1
- Show N_FILTERS more
-
-
-
Scientific topic
- High-throughput sequencing7
- Chromosome walking6
- Clone verification6
- DNA-Seq6
- DNase-Seq6
- High throughput sequencing6
- NGS6
- NGS data analysis6
- Next gen sequencing6
- Next generation sequencing6
- Panels6
- Primer walking6
- Sanger sequencing6
- Sequencing6
- Targeted next-generation sequencing panels6
- Bioinformatics4
- Exomes4
- Genome annotation4
- Genomes4
- Genomics4
- Personal genomics4
- Synthetic genomics4
- Viral genomics4
- Whole genomes4
- Biological sequences2
- Cancer2
- Cancer biology2
- MicroRNA sequencing2
- Neoplasm2
- Neoplasms2
- Oncology2
- RNA sequencing2
- RNA-Seq2
- RNA-Seq analysis2
- Sequence analysis2
- Sequence databases2
- Sequences2
- Small RNA sequencing2
- Small RNA-Seq2
- Small-Seq2
- Transcriptome profiling2
- WTSS2
- Whole transcriptome shotgun sequencing2
- miRNA-seq2
- Allele calling1
- Alternative splicing1
- Antimicrobial stewardship1
- Assembly1
- CNV deletion1
- CNV duplication1
- CNV insertion / amplification1
- Codon usage1
- Communicable disease1
- Comparative transcriptomics1
- Complex CNV1
- Copy number variant1
- Copy number variation1
- DNA chips1
- DNA microarrays1
- DNA polymorphism1
- DNA variation1
- De novo genome sequencing1
- Epidemiology1
- Exome variant detection1
- Expression1
- Gene expression1
- Gene expression profiling1
- Gene transcription1
- Gene translation1
- Genetic variation1
- Genome sequencing1
- Genome variant detection1
- Genomic variation1
- Germ line variant calling1
- Infectious disease1
- Medical microbiology1
- Microbial genetics1
- Microbial physiology1
- Microbial surveillance1
- Microbiological surveillance1
- Microbiology1
- Microsatellites1
- Molecular infection biology1
- Molecular microbiology1
- Mutation1
- Mutation detection1
- Phylogenetic clocks1
- Phylogenetic dating1
- Phylogenetic simulation1
- Phylogenetic stratigraphy1
- Phylogeny1
- Phylogeny reconstruction1
- Pipelines1
- Polymorphism1
- Public health1
- Public health and epidemiology1
- RFLP1
- RNA splicing1
- SNP1
- SNP calling1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses1
- Show N_FILTERS more
-
-
-
Organizer
- BioExcel1
- Show N_FILTERS more
-
-
-
Eligibility
- First come first served1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events