Biotechnology · Moderate · Live online

AI-Assisted CRISPR and CAR-T Cell Engineering for Precision Medicine

Engineering the Future of Precision Medicine with AI, CRISPR, and CAR-T Innovation.

17–19 Aug 20265:30 PM IST3 Days (60-90 minutes)Certificate
The live sessions are over · get the full recording

About This Course

This hands-on workshop explores AI-assisted CRISPR genome editing and CAR-T cell engineering for precision medicine.
Participants will learn computational approaches for guide-RNA design, therapeutic target prioritisation, immune-cell engineering, and AI/ML-based analysis.
The workshop integrates CRISPR, CAR-T, multi-omics, and AI workflows to support next-generation therapeutic research.

Aim

To equip participants with practical skills in therapeutic CRISPR strategy selection, disease-variant analysis, base- and prime-editing design, AI-assisted guide prioritisation, off-target assessment, and sequencing-based evaluation of genome-editing outcomes.

Workshop Objectives

  • Understand therapeutic CRISPR-Cas9, base editing, prime editing, and gene-regulation approaches.
  • Retrieve and interpret disease-associated variants using ClinVar and Ensembl.
  • Select suitable genome-editing strategies for specific variants.
  • Design base-editing guide RNAs and prime-editing pegRNAs.
  • Assess PAM compatibility, editing windows, and bystander mutations.
  • Rank guide candidates using efficiency, specificity, and AI-assisted scoring.
  • Identify and prioritise potential genome-wide off-target sites.
  • Analyse CRISPR amplicon-sequencing data using CRISPResso2.
  • Quantify intended edits, indels, frameshifts, and editing purity.
  • Generate research-oriented figures, summaries, and computational reports.
Next: Day-by-day →

Workshop Structure

📅 Day 1: AI-Guided CRISPR Design for Precision Genome Editing

  • CRISPR-Cas9 mechanism, DNA repair, and genome-editing strategies
  • Target-gene, transcript, exon, and variant selection
  • Guide RNA, PAM, and editing-window principles
  • AI/ML-assisted guide-RNA scoring and prioritisation
  • Base editing and prime editing overview
  • Off-target prediction, specificity, safety, and ethics

🛠️ Hands-on: Target selection, guide-RNA design, computational scoring, and off-target assessment using sample datasets.

🧰 Tools: NCBI Gene, Ensembl, UCSC Genome Browser, UniProt, PubMed, Google Colab, Python, BioPython

📅 Day 2: CRISPR-Supported CAR-T Cell Engineering

  • CAR-T architecture, generations, and therapeutic applications
  • Tumour-antigen selection and target prioritisation
  • Major targets: CD19, BCMA, HER2, EGFR, and MSLN
  • CRISPR-based immune-cell engineering and gene knockout strategies
  • Universal and next-generation CAR-T concepts
  • Antigen escape, T-cell exhaustion, tumour microenvironment, and safety

🛠️ Hands-on: Analyse tumour-antigen expression data, prioritise CAR-T targets, and assess on-target/off-tumour risks.

🧰 Tools: Google Colab, Python, Pandas, NumPy, Matplotlib, Scikit-learn

📅 Day 3: AI-Integrated CRISPR–CAR-T Precision Therapeutics

  • AI-assisted therapeutic target discovery and prioritisation
  • CRISPR screening for resistance genes and therapeutic vulnerabilities
  • Multi-omics and single-cell approaches in precision immunotherapy
  • AI-based therapeutic response and toxicity prediction
  • Next-generation CAR-T: logic-gated, armoured, and universal platforms
  • Translational, regulatory, ethical, and biosafety considerations

🛠️ Hands-on: Build an AI/ML workflow for therapeutic response prediction and interpret key predictive features.

🧰 Tools: Google Colab, Python, Pandas, NumPy, Scikit-learn, Matplotlib, SHAP

Who Should Enrol?

  • UG and PG students in biotechnology, bioinformatics, genetics, genomics, molecular biology, and life sciences
  • Ph.D. scholars, research fellows, faculty members, and academicians
  • Bioinformaticians, computational biologists, and NGS professionals
  • Biotechnology, pharmaceutical, and clinical research professionals
  • Researchers interested in CRISPR, gene therapy, precision medicine, and therapeutic genome editing
Next: Dates →

Important Dates

Registration Ends

August 17, 2026
IST 4:30 PM

Workshop Dates

August 17, 2026 – August 19, 2026
IST 5:30 PM

Workshop Outcomes

  • Interpret disease-associated variants using ClinVar and Ensembl.
  • Select appropriate CRISPR, base-editing, or prime-editing strategies.
  • Design and rank guide RNAs and pegRNAs.
  • Assess PAM compatibility, bystander edits, and off-target risks.
  • Analyse amplicon NGS data using CRISPResso2.
  • Quantify editing efficiency, indels, substitutions, and frameshifts.
  • Prepare research-oriented figures, summaries, and analysis reports.
Next: Fees →

Recording fee

Participants in India

₹2,499

Participants outside India

$50

  • All session recordings
  • Study material
  • Certificate after completion
  • 1-year access

Get the recording

The live sessions of this workshop are over, so the live fees no longer apply. The recordings are being uploaded. They appear in your dashboard as soon as they are ready, and we will e-mail you then.

Next: FAQ →

Frequently asked questions

Will I get the recording?

Yes. Paid participants get the session recordings and study material in their NanoSchool dashboard (My registrations → Recorded Lectures / Study Material).

What if I miss a live session?

Watch the recording in your dashboard and send your questions to the mentor through the support desk.

Do I get a certificate?

Yes, an e-certificate of participation after the workshop, with a QR code anyone can verify and an "Add to LinkedIn" button.

Which fee category applies to me?

Choose the category that matches your current role: Student, Ph.D. Scholar / Researcher, Academician / Faculty or Industry Professional.

How can I pay?

By card, UPI or PayPal on the payment page; international bank transfer is also available there.

What is the refund policy?

See our Returns, Refunds & Cancellation policy: Returns, Refunds & Cancellation policy

Need Help?

We’re here for you!


(+91) 120-4781-217
WhatsApp +91 99581 61117

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