- Home
- Events
Filters
Sort
-
-
Filter Clear filters
-
-
Start
- -
-
-
-
Content provider
- Australian BioCommons1
- Show N_FILTERS more
-
-
-
Scientific topic
- Workflows
- Bioinformatics2
- DNA variation2
- Genetic variation2
- Genomic variation2
- Mutation2
- Polymorphism2
- Somatic mutations2
- Biomarkers1
- Biotherapeutics1
- Cancer1
- Cancer biology1
- Chromosome walking1
- Clone verification1
- DNA-Seq1
- DNase-Seq1
- De novo genome sequencing1
- Diagnostic markers1
- Exomes1
- Genome annotation1
- Genome sequencing1
- Genomes1
- Genomics1
- High throughput sequencing1
- High-throughput sequencing1
- NGS1
- NGS data analysis1
- Neoplasm1
- Neoplasms1
- Next gen sequencing1
- Next generation sequencing1
- Oncology1
- Panels1
- Personal genomics1
- Pipelines1
- Primer walking1
- Sanger sequencing1
- Sequencing1
- Software integration1
- Synthetic genomics1
- Targeted next-generation sequencing panels1
- Tool integration1
- Tool interoperability1
- Viral genomics1
- WGS1
- Whole genome resequencing1
- Whole genome sequencing1
- Whole genomes1
- Show N_FILTERS more
-
-
-
Operation
- Allele calling
- Analysis3
- Biological pathway analysis1
- Biological pathway modelling1
- Biological pathway prediction1
- Ecological modelling1
- Exome variant detection1
- Functional clustering1
- Functional pathway analysis1
- Functional sequence clustering1
- Genome variant detection1
- Germ line variant calling1
- Mutation detection1
- Optimisation and refinement1
- Pathway analysis1
- Pathway comparison1
- Pathway modelling1
- Pathway prediction1
- Pathway simulation1
- Somatic variant calling1
- Variant calling1
- Variant mapping1
- de novo mutation detection1
- Show N_FILTERS more
-
-
-
Event type
- Workshops and courses1
- Show N_FILTERS more
-
-
-
Organizer
- Australian BioCommons1
- Show N_FILTERS more
-
-
-
Eligibility
- First come first served1
- Show N_FILTERS more
-
- Only show online events
- Hide past events
- Show disabled events