Showing 30 materials out of 76
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WEBINAR: Getting started with command line bioinformatics
Computational biology Command line -
WORKSHOP: Variant calling in humans, animals and plants with Galaxy
Genetic variation Variant calling -
WEBINAR: Detection of and phasing of hybrid accessions in a target capture dataset
Phylogenetics Phylogeny -
WEBINAR: Getting started with deep learning
Machine learning Deep learning -
WEBINAR: Making sense of phosphoproteomics data with Phosphomatics
Proteomics Protein modifications Phosphoproteomics -
WEBINAR: Conflict in multi-gene datasets: why it happens and what to do about it - deep coalescence, paralogy and reticulation
Phylogenetics -
Presentation
Make your computational workflows findable and citable: WorkflowHub BYOW workshop
Workflows WorkflowHub FAIR -
WEBINAR: Getting started with spatial omics
Bioinformatics Spatial omics -
WEBINAR: Making sense of gene and protein lists with functional enrichment analysis
Bioinformatics Enrichment analysis -
WEBINAR: Building the future of bioinformatics with Nextflow: Technical innovation, community engagement, and career development opportunities
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WEBINAR: Getting started with proteomics
Bioinformatics Proteomics Mass spectrometry -
WORKSHOP: R: fundamental skills for biologists
Data visualisation Data architecture, analysis and design Bioinformatics Analysis Statistics R software RStudio -
WORKSHOP: Make your bioinformatics workflows findable and citable
Bioinformatics Workflows WorkflowHub FAIR Open Science -
WORKSHOP: Introduction to Metabarcoding using QIIME2
Bioinformatics Analysis Workflows Microbial ecology Metabarcoding Microbiome -
WEBINAR: High performance bioinformatics: submitting your best NCMAS application
Computational Biology Bioinformatics High Performance Computing HPC NCMAS -
WORKSHOP: Making sense of gene and protein lists with functional enrichment analysis
Bioinformatics http://edamontology.org/topic_0091 Analysis http://edamontology.org/operation_2945 Enrichment analysis http://edamontology.org/operation_3501 -
WORKSHOP: Working with genomics sequences and features in R with Bioconductor
R software Bioconductor Bioinformatics Analysis Genomics Sequence analysis -
WEBINAR: Effective, inclusive, and scalable training in the life sciences, clinical education and beyond
Short-format training Clinical education Continuing education Professional development Training Lifelong learning Pedagogy -
WORKSHOP: RNASeq: reads to differential genes and pathways
bioinformatics transcriptomics RNA-seq RNAseq -
WORKSHOP: Single cell RNAseq analysis in R
Bioinformatics Analysis Transcriptomics R software Single cell RNAseq scRNAseq -
WEBINAR: Detection of and phasing of hybrid accessions in a target capture dataset
Phylogenetics Bioinformatics Phylogeny Genomics Target capture sequencing -
WEBINAR: Protection of genomic data and the Australian Privacy Act: when is genomic data 'personal information'?
Bioinformatics Genomics Genetic data Personal information Health information Privacy -
WEBINAR: Portable, reproducible and scalable bioinformatics workflows using Nextflow and Pawsey Nimbus Cloud
Bioinformatics Workflows Nextflow Containerisation -
WEBINAR: Getting started with RNAseq: Transforming raw reads into biological insights
Bioinformatics Transcriptomics RNA-seq RNAseq Gene expression -
WORKSHOP: Machine learning in the life sciences
Bioinformatics Life Science Machine Learning -
WORKSHOP: Fungal Genomics with Galaxy
Bioinformatics Analysis Fungi Genome assembly Genome annotation -
WEBINAR: Using in silico design methods to create de novo proteins that selectively modulate apoptosis
BIoinformatics Proteomics Deep learning Protein design Structural biology -
WEBINAR: DOME - Machine Learning Best Practices & Recommendations
Bioinformatics http://edamontology.org/topic_0091 Machine Learning http://edamontology.org/topic_3474 -
WEBINAR: Getting started with command line bioinformatics
Bioinformatics Command line Workflows Bash Computational biology -
WEBINAR: Getting started with whole genome mapping and variant calling on the command line
Genome mapping Variant calling Bioinformatics Workflows
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