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NGS Library Preparation Fundamentals
Hands-on training in DNA/RNA extraction, fragmentation, and adapter ligation for lab technicians new to NGS workflows.
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Illumina Sequencing Platform Operations
Comprehensive operational training for running Illumina sequencers including cluster generation, imaging, and troubleshooting for technicians.
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PacBio Long-Read Sequencing Techniques
Specialized training in SMRT sequencing technology, library prep, and data collection for researchers working with long reads.
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Oxford Nanopore MinION Workflow
Practical training on portable nanopore sequencing setup, sample preparation, and real-time data analysis for field technicians.
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NGS Data Quality Assessment
Training in evaluating sequencing quality metrics, read distributions, and error patterns for bioinformatics professionals.
15
WORKSHOPS
PROGRAMMES
Read Quality Metrics and FastQC Analysis
3
Adapter Contamination Detection and Removal
3
Sequence Complexity and Low-Quality Base Filtering
3
+2 more programmes
📅 Next: 4 Oct 2026
🎟 4320 seats open
🎓 Professional
🏢 15 offline
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Fastq File Analysis and Interpretation
Hands-on workshop on reading, parsing, and troubleshooting fastq files for bioinformaticians and data analysts.
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Genome Assembly from NGS Data
Advanced training in de novo and reference-based assembly algorithms using industry-standard tools for bioinformaticians.
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Variant Calling and SNP Detection
Comprehensive training in identifying genetic variants, annotation, and filtering for clinical and research genomicists.
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RNA-Seq Expression Analysis
Practical training in quantifying gene expression, normalization, and differential expression analysis for researchers.
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Whole Genome Sequencing WGS Protocols
Complete WGS workflow training from sample preparation through analysis for clinical and research professionals.
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Whole Exome Sequencing WES Techniques
Specialized training in exome capture, enrichment, and analysis for clinical diagnostics and research applications.
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Targeted Panel Sequencing Design
Training in designing custom gene panels, probe design, and targeted sequencing optimization for specialized applications.
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ChIP-Seq Data Analysis and Interpretation
Advanced workshop on chromatin immunoprecipitation sequencing analysis for epigenomics researchers and bioinformaticians.
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ATAC-Seq Chromatin Accessibility
Training in assay for transposase-accessible chromatin sequencing methodology and data interpretation for epigenetics specialists.
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Single-Cell RNA-Seq scRNA-Seq
Comprehensive training in single-cell transcriptomics workflows, cell clustering, and cell type identification for advanced researchers.
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Microbiome Sequencing and Analysis
Practical training in 16S rRNA and metagenomic sequencing for microbiome composition and diversity analysis.
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Bioinformatics Pipeline Development
Advanced training in building automated NGS analysis pipelines using Nextflow, Snakemake, or CWL for bioinformaticians.
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NGS Data Management and Storage
Training in handling large-scale genomic data, storage solutions, backup strategies, and data security for IT and lab managers.
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GATK Variant Analysis Toolkit
Hands-on training in the Genome Analysis Toolkit for variant discovery and genotyping for genomics professionals.
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SAMtools and BAM File Manipulation
Practical workshop on manipulating, filtering, and analyzing BAM files using SAMtools for bioinformaticians.
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IGV Genome Browser Visualization
Training in using Integrative Genomics Viewer for visualizing and interpreting genomic data for researchers.
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R Programming for NGS Analysis
Programming training in R language using Bioconductor packages for NGS data analysis and visualization.
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Python for Bioinformatics
Practical Python programming training for NGS data processing, scripting, and analysis automation.
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Clinical NGS Report Interpretation
Training for clinicians and genetic counselors on interpreting NGS results and communicating findings to patients.
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NGS Quality Control Best Practices
Comprehensive training in QC protocols, standards, and troubleshooting for maintaining sequencing quality.
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NGS Laboratory Safety Protocols
Essential safety training for NGS lab personnel covering chemical, biological, and equipment hazards.
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NGS Contamination Detection Prevention
Practical training in identifying and preventing sample contamination in NGS workflows for lab technicians.
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NGS Compliance and Regulatory Standards
Training in CLIA, CAP, ISO, and other regulatory requirements for clinical NGS laboratories.
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Next-Gen Sequencer Maintenance
Hands-on technical training in routine maintenance, troubleshooting, and repair of NGS instruments.
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NGS Cost Analysis and Optimization
Training for laboratory managers on optimizing NGS costs, throughput, and resource allocation.
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Copy Number Variation Detection
Advanced training in detecting and analyzing copy number variations from NGS data for clinical applications.
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Structural Variant Identification
Specialized training in detecting large genomic rearrangements and structural variations from NGS data.
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Somatic Mutation Analysis
Training in identifying cancer-related somatic mutations and clonal evolution from tumor sequencing data.
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Pharmacogenomics NGS Applications
Training in using NGS for drug metabolism and response predictions in personalized medicine applications.
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Prenatal and Carrier Screening
Specialized training in NGS-based prenatal diagnosis and carrier screening interpretation for genetic counselors.
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Infectious Disease Pathogen Detection
Training in using NGS for rapid pathogen identification and antimicrobial resistance profiling in clinical settings.
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HLA Typing and Immunogenomics
Specialized training in high-resolution HLA typing and immune repertoire analysis using NGS.
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Liquid Biopsy Cell-Free DNA Analysis
Advanced training in ctDNA and cfDNA analysis for early cancer detection and monitoring.
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De Novo Mutation Analysis
Training for geneticists in identifying and validating de novo variants in familial disease studies.
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NGS Workflow Optimization
Training for laboratory managers on streamlining NGS processes to improve efficiency and reduce turnaround time.
15
WORKSHOPS
PROGRAMMES
Demultiplexing & Quality Control in NGS Pipelines
3
Alignment Optimization & Reference Genome Selection
3
Variant Calling Pipelines: Germline & Somatic Integration
3
+2 more programmes
📅 Next: 4 Oct 2026
🎟 4380 seats open
🏢 15 offline
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Bioinformatics Team Leadership
Management training for bioinformatics supervisors overseeing NGS data analysis teams and projects.
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NGS Troubleshooting and Problem-Solving
Advanced diagnostic training for resolving sequencing failures and data quality issues.
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Statistical Analysis NGS Data
Training in statistical methods and significance testing for genomic data analysis professionals.
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Linux and Command-Line Bioinformatics
Foundational training in Linux operating systems and command-line tools for NGS analysis.
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NGS Data Visualization Techniques
Training in creating effective visualizations and figures from genomic data for presentations and publications.
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High-Throughput Screening Integration
Training in integrating NGS with high-throughput screening platforms for large-scale variant analysis.
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Ancient DNA and Degraded Sample Analysis
Specialized training in handling and analyzing low-quality or damaged DNA from archaeological samples.
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NGS for Plant Genomics
Practical training in applying NGS techniques to crop improvement and plant breeding applications.
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Veterinary NGS Applications
Training in NGS use for animal genetics, disease diagnosis, and breeding programs in veterinary medicine.
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Metagenomics and Environmental Sequencing
Training in sequencing environmental samples to characterize microbial and biological communities.
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