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Functional Genomics Workshops

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Showing 13–24 of 50 categories
Transcriptome Assembly and Reconstruction
Advanced workshop on transcript assembly, isoform detection, and novel gene discovery for bioinformaticians.
3+WORKSHOPS
PROGRAMMES
De Novo Transcriptome Assembly with Trinity Genome Guided Transcript Reconstruction Workflows RNA-Seq Quality Control and Read Preprocessing +2 more programmes
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Pathway Analysis and Network Interpretation
Training on functional enrichment analysis, pathway databases, and biological network visualization for genomics professionals.
3+WORKSHOPS
PROGRAMMES
KEGG Pathway Mapping and Functional Annotation Gene Regulatory Network Reconstruction from RNA-seq Systems Biology Network Analysis and Visualization +2 more programmes
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Chromatin Immunoprecipitation Sample Prep
Hands-on laboratory training on ChIP sample preparation, antibody selection, and quality control for molecular technicians.
3+WORKSHOPS
PROGRAMMES
ChIP Sample Preparation Quality Control Essentials Chromatin Fragmentation and Sonication Protocol Mastery Immunoprecipitation Optimization for ChIP Workflows +2 more programmes
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Digital PCR ddPCR Advanced Applications
Specialized training on droplet digital PCR setup, optimization, and data analysis for molecular diagnostics specialists.
3+WORKSHOPS
PROGRAMMES
Digital PCR Absolute Quantification Without Standard Curves Copy Number Variation Detection Using Droplet Digital PCR Rare Mutation Detection and Minimal Residual Disease Monitoring +2 more programmes
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Next-Generation Sequencing Quality Control
Comprehensive workshop on NGS library quality metrics, sequencing QC parameters, and troubleshooting for lab technicians.
3+WORKSHOPS
PROGRAMMES
NGS Data Quality Assessment and Filtering Read Alignment Quality Control and Validation Variant Calling Quality Metrics and Benchmarking +2 more programmes
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Bioinformatic Pipeline Development Tools
Training on Nextflow, Snakemake, and workflow management systems for bioinformaticians building automated analysis pipelines.
3+WORKSHOPS
PROGRAMMES
Building RNA-seq Analysis Pipelines with Nextflow Variant Calling Pipeline Development and Optimization Containerizing Bioinformatic Workflows with Docker and Singularity +2 more programmes
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Copy Number Variation Detection Methods
Advanced training on CNV identification from sequencing and microarray data for genomic analysts and geneticists.
3+WORKSHOPS
PROGRAMMES
CNV Detection Using Next Generation Sequencing Array CGH Data Analysis and Interpretation Digital PCR for Copy Number Quantification +2 more programmes
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Epigenetic Modifications Mapping Techniques
Specialized workshop on DNA methylation, histone modification analysis, and bisulfite sequencing for epigenomics researchers.
3+WORKSHOPS
PROGRAMMES
ChIP-seq Data Analysis and Peak Calling ATAC-seq Accessibility Mapping and Interpretation DNA Methylation Profiling with Bisulfite Sequencing +2 more programmes
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Library Preparation Methods for Sequencing
Practical hands-on training on RNA and DNA library construction, fragmentation, and adapter ligation for molecular technicians.
3+WORKSHOPS
PROGRAMMES
RNA Extraction and Quality Assessment Protocols mRNA Enrichment and cDNA Synthesis Methods Adapter Ligation and Index Assignment Workflows +2 more programmes
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Metagenomics and Microbiome Analysis
Training on environmental DNA analysis, taxonomic classification, and microbiome functional profiling for environmental genomicists.
3+WORKSHOPS
PROGRAMMES
16S rRNA Amplicon Sequencing Data Processing Shotgun Metagenomic Assembly and Binning Functional Annotation of Metagenomic Sequences +2 more programmes
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Gene Ontology and Functional Databases
Workshop on leveraging Gene Ontology, UniProt, and functional databases for protein and gene annotation for researchers.
3+WORKSHOPS
PROGRAMMES
Gene Ontology Annotation and Data Interpretation Querying Functional Databases for Genomic Research Enrichment Analysis Using Gene Ontology Terms +2 more programmes
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Structural Variation SV Detection Analysis
Advanced training on large-scale chromosomal rearrangement detection and interpretation in genomic datasets.
3+WORKSHOPS
PROGRAMMES
Detecting Structural Variations Using Long Read Sequencing Short Read SV Discovery With Paired End Mapping Validating and Annotating Structural Variants Systematically +2 more programmes
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