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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.
15WORKSHOPS
PROGRAMMES
Read Quality Metrics and FastQC Analysis3Adapter Contamination Detection and Removal3Sequence Complexity and Low-Quality Base Filtering3+2 more programmes
📅 Next: 4 Oct 2026🎟 4320 seats open🎓 Professional
🏢 15 offlineExplore workshops →
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.
15WORKSHOPS
PROGRAMMES
Demultiplexing & Quality Control in NGS Pipelines3Alignment Optimization & Reference Genome Selection3Variant Calling Pipelines: Germline & Somatic Integration3+2 more programmes
📅 Next: 4 Oct 2026🎟 4380 seats open
🏢 15 offlineExplore workshops →
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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