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Bioinformatics Workshops

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Showing 13–24 of 50 categories
ChIP-Seq and Epigenomics Analysis
Specialist workshop for researchers analyzing chromatin immunoprecipitation and epigenetic modification data using peak calling and motif discovery tools.
3+WORKSHOPS
PROGRAMMES
ChIP-Seq Peak Calling and Quality Control Epigenetic Histone Modification Mapping Workflows Multi-Sample ChIP-Seq Comparative Analysis +2 more programmes
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Single Cell Genomics and Analysis
Cutting-edge training for interpreting single-cell RNA-seq, scATAC-seq data, and performing cell clustering and annotation workflows.
3+WORKSHOPS
PROGRAMMES
10X Genomics Data Processing and Quality Control Single Cell RNA-seq Clustering and Cell Type Annotation Single Cell ATAC-seq Analysis and Peak Calling +2 more programmes
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Pathway and Network Analysis Methods
Training for systems biologists to perform gene set enrichment, biological pathway mapping, and protein-protein interaction network analysis.
3+WORKSHOPS
PROGRAMMES
Protein Interaction Network Reconstruction and Analysis KEGG Pathway Mapping and Functional Enrichment Systems Biology Network Modeling and Simulation +2 more programmes
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Phylogenetic Analysis and Tree Building
Hands-on course for evolutionary biologists constructing phylogenetic trees, performing sequence alignment, and interpreting evolutionary relationships.
3+WORKSHOPS
PROGRAMMES
Maximum Likelihood Estimation in Phylogenetic Inference Bayesian Phylogenetics and MCMC Tree Sampling Molecular Clock Calibration and Dating Phylogenies +2 more programmes
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Molecular Docking and Drug Discovery
Specialist training for computational chemists performing molecular docking, virtual screening, and ligand-protein interaction predictions.
3+WORKSHOPS
PROGRAMMES
Protein Structure Preparation for Molecular Docking Virtual Screening and Lead Compound Identification RMSD Analysis and Docking Pose Validation +2 more programmes
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Quality Control in NGS Data
Technical certification for QC technicians implementing quality metrics, identifying sequencing artifacts, and ensuring data reliability in next-generation sequencing.
3+WORKSHOPS
PROGRAMMES
FastQC and Multiqc Pipeline Implementation Adapter Trimming and Read Filtering Strategies Coverage Analysis and Depth Profiling Methods +2 more programmes
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Bioinformatics Data Visualization
Creative training for scientists creating interactive dashboards, heatmaps, and 3D visualizations for complex genomic and proteomic datasets.
3+WORKSHOPS
PROGRAMMES
3D Protein Structure Visualization and PyMOL Mastery Interactive Genomic Data Visualization with R and Shiny NGS Data Quality Control and Multi-dimensional Analysis +2 more programmes
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CRISPR Target Prediction and Design
Advanced workshop for molecular biologists designing CRISPR guide RNAs, predicting off-target effects, and optimizing genome editing experiments.
3+WORKSHOPS
PROGRAMMES
Off-target Effects Prediction and Mitigation Strategies PAM Sequence Analysis for Expanded CRISPR Toolkit Machine Learning Models for sgRNA Efficacy Prediction +2 more programmes
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Copy Number Variation Detection
Specialized training for clinical genomics professionals identifying and interpreting copy number variations using CNV calling algorithms.
3+WORKSHOPS
PROGRAMMES
CNV Detection Using Next Generation Sequencing Array CGH Data Analysis and Interpretation Whole Genome Sequencing CNV Calling Pipelines +2 more programmes
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Transcription Factor Binding Site Analysis
Technical course teaching regulatory biologists to identify and analyze transcription factor binding motifs and gene regulatory elements.
3+WORKSHOPS
PROGRAMMES
ChIP-seq Data Processing and Peak Calling Motif Discovery and Pattern Recognition Algorithms Machine Learning for TFBS Prediction Models +2 more programmes
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Clinical Variant Interpretation Standards
Compliance-focused training for clinical laboratory technicians applying ACMG guidelines and interpreting variants for diagnostic purposes.
3+WORKSHOPS
PROGRAMMES
ACMG Guidelines Implementation in Variant Classification VEP and Ensembl Annotation for Clinical Genomics ClinVar Database Curation and Evidence Integration +2 more programmes
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Whole Exome Sequencing Interpretation
Clinical genetics training for identifying disease-causing variants in coding regions, filtering strategies, and medical reporting protocols.
3+WORKSHOPS
PROGRAMMES
Variant Annotation and Pathogenicity Assessment Workflows Copy Number Variation Detection in WES Data Analysis Quality Control and Read Mapping Optimization Strategies +2 more programmes
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How Bioinformatics Workshops Work

The workshop structure is simple and consistent. At the top sit categories that group related bioinformatics topics. Within each category are individual workshop programmes focused on a single theme. And every programme is offered in exactly three fixed variants, each tuned to a specific audience. To attend, you move from category, to programme, to the variant that matches your level.

Categories, Programmes & Variants

Think of it as three layers. The category tells you the broad area; the programme is the specific workshop you join; and the variant sets the depth and pace. This keeps a large catalogue easy to navigate and ensures every learner lands at the right level.

Variant 1 — School Students (Classes 9–12)

This variant introduces bioinformatics from the ground up — what biological data is, how computers help read DNA and why it matters to medicine and biology. The language is plain, the demonstrations are visual and the aim is to spark curiosity and build a solid conceptual base for science and computing study ahead.

Variant 2 — UG & PG College Students

Pitched at undergraduate and postgraduate learners, this variant is applied and tool-oriented. It connects syllabus concepts to practice — running BLAST, aligning sequences, a first script — reinforcing coursework while adding employable computational ability.

Variant 3 — Professionals & Research Scholars

The advanced variant targets working professionals and scholars. It goes deeper into method and current tools — pipeline practice, NGS analysis nuance or research-relevant techniques — assuming an existing foundation and focusing on sharpening or updating it.

The Kinds of Topics Covered

Workshops address sharply defined skills — running a BLAST search, performing a multiple sequence alignment, building a phylogenetic tree, writing a basic Biopython or R script or navigating a biological database. Each programme isolates one such topic so the session stays focused and useful.

Short Format, Single Focus

Workshops are intensive and compact by design. Rather than spanning weeks, they concentrate on one tool or concept in a single sharp session, making them easy to fit around school, college or work.

Online & Offline Delivery

Workshops run online for reach and convenience and offline at the lab for guided, hands-on practice with setup support. The variant you choose sets the depth; the mode you choose sets how you attend.

Practical & Interactive

Sessions are participatory. You work through the tool or analysis alongside the facilitator rather than only watching, so the takeaway is a skill you have actually practised — not just notes to read later.

Who Should Attend

There is a fit for almost everyone: school students exploring science and computing, college students reinforcing coursework, and professionals or scholars updating a specific tool. The three-variant design means each person joins at the right depth.

What You Take Away

You leave with a concrete skill, worked examples to revisit and a participation certificate. Because the commitment is small, workshops are also a smart way to test interest before investing in fuller training.

A Stepping Stone

Workshops act as an on-ramp. A tool that interests you in a short session can be pursued further through structured training, a project or an internship — the workshop is the low-risk first step.

Certification

Participants receive a verifiable certificate recording the workshop and variant attended — a useful addition to a school portfolio, college record or professional profile.

Why Three Variants Matter

A single session cannot serve a 15-year-old and a practising researcher equally. By fixing three variants per programme, each session is pitched, paced and demonstrated for its audience, so no one is lost and no one is bored.

Explore Workshop Categories

Bioinformatics workshops are grouped into categories that lead to individual programmes, each available in the three fixed variants. Explore the categories below to choose a topic and the variant that fits you.