- Home
- Events
Filter
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- EMBL-ABR2
- IFB French Institute of Bioinformatics2
- Show N_FILTERS more
-
-
-
Keyword
- bioinformatics
- Galaxy4
- RNA-Seq4
- RNA-seq4
- Transcriptomics4
- Bioinformatics3
- Gene Expression3
- RNA-Seq2
- ChIP-seq2
- HDRUK2
- RNASeq2
- Single Cell Genomics2
- Variant detection2
- next-generation sequencing2
- scRNAseq2
- R-programming1
- ABR1
- Bioconductor1
- Cross domain (cross-domain)1
- DNA & RNA (dna-rna)1
- Data analysis1
- Databases1
- Differential Expression1
- Droplet-based single-cell RNA library preparation1
- ELIXIR1
- Expression Atlas1
- Functional analysis1
- Galaxy Australia1
- Gene expression1
- Gene expression (gene-expression)1
- HCA data portal1
- High Throughput Sequencing Analysis1
- Human Cell Atlas Data Coordination Platform1
- Mapping1
- Molecular building blocks of life1
- NGS1
- Next generation sequencing data analysis1
- Nextflow1
- Pathway analysis1
- Quality Control1
- R software1
- RNA sequencing1
- RNAseq1
- Sequence Analysis1
- Seurat1
- Single Cell technologies1
- Single cell1
- Single-cell transcriptomics1
- TtT, Train the Trainer, Educational psychology, cognitive science, teaching practices 1
- VLSCI1
- Workflows1
- nf-core1
- omics1
- python1
- scRNA-seq1
- single cell RNA-seq analysis1
- tidyverse1
- Show N_FILTERS more
-
-
-
Scientific topic
- Small-Seq
- Bioinformatics116
- Exomes6
- Genome annotation6
- Genomes6
- Genomics6
- Personal genomics6
- Synthetic genomics6
- Viral genomics6
- Whole genomes6
- Biomathematics4
- Chromosome walking4
- Clone verification4
- Computational biology4
- DNA-Seq4
- DNase-Seq4
- Data management4
- High throughput sequencing4
- High-throughput sequencing4
- Mathematical biology4
- Metadata management4
- MicroRNA sequencing4
- NGS4
- NGS data analysis4
- Next gen sequencing4
- Next generation sequencing4
- Panels4
- Primer walking4
- RNA sequencing4
- RNA-Seq4
- RNA-Seq analysis4
- Research data management (RDM)4
- Sanger sequencing4
- Sequencing4
- Small RNA sequencing4
- Small RNA-Seq4
- Targeted next-generation sequencing panels4
- Theoretical biology4
- Transcriptome profiling4
- WTSS4
- Whole transcriptome shotgun sequencing4
- miRNA-seq4
- Pipelines3
- Software integration3
- Tool integration3
- Tool interoperability3
- Workflows3
- Active learning2
- ChIP-exo2
- ChIP-seq2
- ChIP-sequencing2
- Chip Seq2
- Chip sequencing2
- Chip-sequencing2
- DNA variation2
- Data integration2
- Data integration and warehousing2
- Data warehousing2
- De novo genome sequencing2
- Ensembl learning2
- Genetic variation2
- Genome sequencing2
- Genomic variation2
- Kernel methods2
- Knowledge representation2
- Machine learning2
- Mutation2
- Neural networks2
- Polymorphism2
- Recommender system2
- Reinforcement learning2
- Somatic mutations2
- Supervised learning2
- Unsupervised learning2
- WGS2
- Whole genome resequencing2
- Whole genome sequencing2
- Aerobiology1
- Bayesian methods1
- Behavioural biology1
- Biological rhythms1
- Biological science1
- Biology1
- Biostatistics1
- Bottom-up proteomics1
- Chemical informatics1
- Cheminformatics1
- Chemoinformatics1
- Chronobiology1
- Cloud computing1
- Comparative transcriptomics1
- Computational ecology1
- Computer science1
- Cryobiology1
- Data mining1
- Data rendering1
- Data visualisation1
- Descriptive statistics1
- Diffraction experiment1
- Discovery proteomics1
- 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
- Australia2
- France2
- Show N_FILTERS more
-
-
-
Eligibility
- Registration of interest2
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events