Virtual course
Cancer genomics and transcriptomics
2025
This course will focus on the analysis of data from genomic studies of cancer. It will also highlight the application of transcriptomic analysis and single-cell technologies in cancer. Talks and interactive sessions will give an insight into the bioinformatic concepts required to analyse such data, whilst practical sessions will enable the participants to apply statistical methods to the analysis of cancer genomics data under the guidance of the trainers.
Virtual course
Participants will learn via a mix of pre-recorded lectures, live presentations, and trainer Q&A sessions. Practical experience will be developed through group activities and trainer-led computational exercises. Live sessions will be delivered using Zoom with additional support and asynchronous communication via Slack.
Pre-recorded material may be provided before the course starts that participants will need to watch, read or work through to gain the most out of the actual training event. In the week before the course, there will be a brief induction session. Computational practicals will run on EMBL-EBI's virtual training infrastructure, meaning participants will not require access to a powerful computer or install complex software on their own machines.
Participants will need to be available between the hours of 08:45 – 17:30 BST each day of the course. Trainers will be available to assist, answer questions, and provide further explanations during these times.
Who is this course for?
We welcome applications from PhD students, post-doc researchers, and those working in industry. This course is well-suited for those who are applying, or planning to apply, high throughput sequencing and single-cell technologies in cancer research and wish to familiarise themselves with bioinformatics tools and data analysis methodologies specific to cancer data.
Familiarity with the technology and biological use cases of high throughput sequencing (HTS) is required, as is some experience with R/Bioconductor (basic understanding of the R syntax and ability to manipulate R objects) and the Unix/Linux operating system. There are many tutorials available online and here are some that may be of help:
To complete the following suggested tutorials you may want to install Ubuntu for Windows Users if you are using a computer with a Windows Operating System.
We recommend these free tutorials:
Regardless of your current knowledge, we encourage successful participants to use these, and other materials, to prepare for attending the course and future work in this area.
What will I learn?
Course content
During this course you will learn about:
- Application of high throughput sequencing (HTS) in cancer
- Introduction to cancer genomics and epigenetics
- Structural variation, SNV and CNV analysis, and data visualisation
- Application of CRISPR-Cas9 genome editing in studying cancer
- RNA-seq analysis (both short and long reads)
- Single-cell research in cancer
Learning outcomes
After the course you should be able to:
- Evaluate the applications and challenges of HTS in the study of cancer genomics
- Detect, visualise, and annotate copy number variation
- Interpret complex genomic rearrangements such as structural variants
- Explain the principles of tumour purity, heterogeneity, and evolution and how we detect or quantify them using bioinformatic approaches
- Explore the application of CRISPR-Cas9 genome editing in cancer studies
- Perform alignment and quantification of expression of RNA-seq datasets
- Explore the application of single-cell sequencing in cancer studies
Trainers
Patricia Basurto Lozada
LIIGH-UNAM Saul Carcamo
Icahn School of Medicine at Mount Sinai Kenya Contreras Ramírez
EMBL-EBI Deniz Demircioglu
Icahn School of Medicine at Mount Sinai Francesco Iorio
Human Technopole Alexey Larionov
Cranfield University Gabriel Pereira
Universidade Federal de Ciências da Saúde de Porto Alegre Tobias Rausch
EMBL Heidelberg Carla Daniela Robles-Espinoza
LIIGH-UNAM Estef Vázquez
LIIGH-UNAM
Programme
All times in the programme are listed in BST. Programme is subject to minor changes.
Time
Topic
Trainer
Day one – Monday 12 May 2025
09:00 — 09:45
Welcome and introductions
Patricia Carvajal-López
09:45 — 10:45
Introduction to cancer genomics and its caveats
Tobias Rausch
10:45 — 11:00
Break
11:00 — 12:30
Introduction to cancer genomics and its caveats
Tobias Rausch
12:30 — 13:30
Lunch break
13:30 — 14:30
High-throughput sequencing and single-nucleotide variant analysis in cancer
Daniela Robles-Espinoza
14:30 — 15:00
Flash talks
15:00 — 17:00
Practical: Alignment and SNV analysis
Daniela Robles-Espinoza, Patricia Basurto and Kenya Contreras Ramirez
17:00
End of day
Day two – Tuesday 13 May 2025
08:45 — 09:00
Morning challenge
09:00 — 09:45
Structural and copy-number variation analysis
Tobias Rausch
09:45 — 10:30
Mutational processes and clonal population structure in cancer genomes
Tobias Rausch
10:30 — 11:00
Break
11:00 — 12:00 Interrogating cancer genomes using long reads
Tobias Rausch 12:00 — 13:30
Lunch break and group photo
13:00 — 15:30
Practicals: SV/CNV analysis using short-reads
Tobias Rausch
15:30 — 15:45
Break
15:45 — 17:00
Flash talks
17:00
End of day
Day three – Wednesday 14 May 2025
08:45 — 09:00
Morning challenge
09:00 — 10:00
Short-read RNA-seq analysis
Alexey Larionov
10:00 — 10:20
Break
10:20 — 12:30
Short-read RNA-seq analysis (practicals and troubleshooting)
Alexey Larionov
12:30 — 14:00
Lunch break
14:00 — 15:30
Introduction to single-cell technologies in cancer genomics
Deniz Demircioglu
15:30 — 16:00
Break
16:00 — 17:30
Practicals and troubleshooting
Deniz Demircioglu
17:30
End of day
Day four – Thursday 15 May 2025
08:45 — 09:00
Morning challenge
09:00 — 10:30
CRISPR-Cas9 genome editing for identifying cancer dependencies and new therapeutic targets
Francesco Iorio
10:30 — 10:45
Break
10:45 — 12:30
Pre-processing, QC assessment, and visualisation of gene essentiality profiles from CRISPR-Cas9 screens (practicals and troubleshooting)
Francesco Iorio
12:30 — 13:30
Lunch break
13:30 — 14:30
Epigenetics
Saul Carcamo
14:30 — 15:00
Break
15:00 — 17:00
Epigenetics: practical
Saul Carcamo
17:00
End of day
Day five – Friday 16 May 2025
08:45 — 09:00
Morning challenge
09:00 — 10:00
Long-read RNA-seq analysis
Alexey Larionov
10:00 — 10:15
Break
10:15 — 12:00
Long-read RNA-seq analysis (practicals and troubleshooting)
Alexey Larionov
12:00 — 13:00
Lunch break
13:00 — 14:00
Practical: deconvolution of the clonality of a tumour using single-cell transcriptomic data
Estefania Vázquez and Gabriel Pereira
14:00 — 14:30
Break
14:30 — 16:00
Practical: deconvolution of the clonality of a tumour using single-cell transcriptomic data
Estefania Vázquez and Gabriel Pereira
16:00 — 16:30
Course wrap-up and feedback
Patricia Carvajal-López
Please read our support page before starting your application. In order to be considered for a place on this course, you must do the following:
- Complete the online application form.
- Ensure you add relevant information to the ‘submission details’ section where you are asked to provide information on your:
- pre-requisite skills and knowledge
- current work and course expectations
- data availability
- Upload one letter of support from your supervisor or a senior colleague detailing reasons why you should be selected for the course.
Please submit all documents during the application process by 23:59 on 9 February 2025. Items marked * in the application are mandatory. Incomplete applications will not be processed.
All applicants will be informed of the status of their application (successful, waiting list, unsuccessful) by 24 February 2025. If you have any questions regarding the application process please contact Anca Belu.
Registration fees
The registration fee includes:
- access to the full five-day course programme
- access to a bespoke online course handbook
- secure community space on Slack
- virtual machine to work on that is accessed via the internet
- dedicated online support team
- certificate on completion of the course
Academia
£225
Industry
£325
Financial assistance
Financial assistance is available for a limited number of participants on this course.
Registration fee waivers
We are able to offer a limited number of registration fee waivers for this course. If you receive a waiver, your registration fee will be reimbursed after you have completed the course.
You will need to apply for the fee waiver at the same time as submitting your application for the course, explaining why you require the waiver and how attending this course will benefit your career.
You will be informed about whether you have received the waiver at the same time as you hear about the application outcome for the course. If your course application is successful, you will need to pay the registration fee at the time you register. You will receive the waiver within a month of submitting your form.
Terms and conditions
The scientific organisers will select the recipients of financial assistance during the course application selection process. Selection for financial support is based on scientific merit, your current work study or location, the reasons for needing financial support and the impact this event will have on your career. Priority will be given to applications from low and middle income countries.
Application for financial support will not affect the outcome of your course application.
Course materials
The 2024 course materials are now live and available for you to use. They provide a mixture of pre-recorded lectures, presentations, and practicals from the course, and will give you a snapshot of what to expect in the 2025 edition.
Flash talks
All participants will be asked to give a short presentation about their research work as part of the course. These provide an opportunity to share their research with the other participants and provide a forum for discussion. Successful applicants will be required to submit their talks upon registration.
LIIGH-UNAM
Icahn School of Medicine at Mount Sinai
EMBL-EBI
Icahn School of Medicine at Mount Sinai
Human Technopole
Cranfield University
Universidade Federal de Ciências da Saúde de Porto Alegre
EMBL Heidelberg
LIIGH-UNAM
LIIGH-UNAM
Programme
All times in the programme are listed in BST. Programme is subject to minor changes.
Time | Topic | Trainer |
Day one – Monday 12 May 2025 | ||
09:00 — 09:45 | Welcome and introductions | Patricia Carvajal-López |
09:45 — 10:45 | Introduction to cancer genomics and its caveats | Tobias Rausch |
10:45 — 11:00 | Break | |
11:00 — 12:30 | Introduction to cancer genomics and its caveats | Tobias Rausch |
12:30 — 13:30 | Lunch break | |
13:30 — 14:30 | High-throughput sequencing and single-nucleotide variant analysis in cancer | Daniela Robles-Espinoza |
14:30 — 15:00 | Flash talks | |
15:00 — 17:00 | Practical: Alignment and SNV analysis | Daniela Robles-Espinoza, Patricia Basurto and Kenya Contreras Ramirez |
17:00 | End of day | |
Day two – Tuesday 13 May 2025 | ||
08:45 — 09:00 | Morning challenge | |
09:00 — 09:45 | Structural and copy-number variation analysis | Tobias Rausch |
09:45 — 10:30 | Mutational processes and clonal population structure in cancer genomes | Tobias Rausch |
10:30 — 11:00 | Break | |
| 11:00 — 12:00 | Interrogating cancer genomes using long reads | Tobias Rausch |
12:00 — 13:30 | Lunch break and group photo | |
13:00 — 15:30 | Practicals: SV/CNV analysis using short-reads | Tobias Rausch |
15:30 — 15:45 | Break | |
15:45 — 17:00 | Flash talks | |
17:00 | End of day | |
Day three – Wednesday 14 May 2025 | ||
08:45 — 09:00 | Morning challenge | |
09:00 — 10:00 | Short-read RNA-seq analysis | Alexey Larionov |
10:00 — 10:20 | Break | |
10:20 — 12:30 | Short-read RNA-seq analysis (practicals and troubleshooting) | Alexey Larionov |
12:30 — 14:00 | Lunch break | |
14:00 — 15:30 | Introduction to single-cell technologies in cancer genomics | Deniz Demircioglu |
15:30 — 16:00 | Break | |
16:00 — 17:30 | Practicals and troubleshooting | Deniz Demircioglu |
17:30 | End of day | |
Day four – Thursday 15 May 2025 | ||
08:45 — 09:00 | Morning challenge | |
09:00 — 10:30 | CRISPR-Cas9 genome editing for identifying cancer dependencies and new therapeutic targets | Francesco Iorio |
10:30 — 10:45 | Break | |
10:45 — 12:30 | Pre-processing, QC assessment, and visualisation of gene essentiality profiles from CRISPR-Cas9 screens (practicals and troubleshooting) | Francesco Iorio |
12:30 — 13:30 | Lunch break | |
13:30 — 14:30 | Epigenetics | Saul Carcamo |
14:30 — 15:00 | Break | |
15:00 — 17:00 | Epigenetics: practical | Saul Carcamo |
17:00 | End of day | |
Day five – Friday 16 May 2025 | ||
08:45 — 09:00 | Morning challenge | |
09:00 — 10:00 | Long-read RNA-seq analysis | Alexey Larionov |
10:00 — 10:15 | Break | |
10:15 — 12:00 | Long-read RNA-seq analysis (practicals and troubleshooting) | Alexey Larionov |
12:00 — 13:00 | Lunch break | |
13:00 — 14:00 | Practical: deconvolution of the clonality of a tumour using single-cell transcriptomic data | Estefania Vázquez and Gabriel Pereira |
14:00 — 14:30 | Break | |
14:30 — 16:00 | Practical: deconvolution of the clonality of a tumour using single-cell transcriptomic data | Estefania Vázquez and Gabriel Pereira |
16:00 — 16:30 | Course wrap-up and feedback | Patricia Carvajal-López |
Please read our support page before starting your application. In order to be considered for a place on this course, you must do the following:
- Complete the online application form.
- Ensure you add relevant information to the ‘submission details’ section where you are asked to provide information on your:
- pre-requisite skills and knowledge
- current work and course expectations
- data availability
- Upload one letter of support from your supervisor or a senior colleague detailing reasons why you should be selected for the course.
Please submit all documents during the application process by 23:59 on 9 February 2025. Items marked * in the application are mandatory. Incomplete applications will not be processed.
All applicants will be informed of the status of their application (successful, waiting list, unsuccessful) by 24 February 2025. If you have any questions regarding the application process please contact Anca Belu.
Registration fees
The registration fee includes:
- access to the full five-day course programme
- access to a bespoke online course handbook
- secure community space on Slack
- virtual machine to work on that is accessed via the internet
- dedicated online support team
- certificate on completion of the course
Academia | £225 |
Industry | £325 |
Financial assistance
Financial assistance is available for a limited number of participants on this course.
Registration fee waivers
We are able to offer a limited number of registration fee waivers for this course. If you receive a waiver, your registration fee will be reimbursed after you have completed the course.
You will need to apply for the fee waiver at the same time as submitting your application for the course, explaining why you require the waiver and how attending this course will benefit your career.
You will be informed about whether you have received the waiver at the same time as you hear about the application outcome for the course. If your course application is successful, you will need to pay the registration fee at the time you register. You will receive the waiver within a month of submitting your form.
Terms and conditions
The scientific organisers will select the recipients of financial assistance during the course application selection process. Selection for financial support is based on scientific merit, your current work study or location, the reasons for needing financial support and the impact this event will have on your career. Priority will be given to applications from low and middle income countries.
Application for financial support will not affect the outcome of your course application.
Course materials
The 2024 course materials are now live and available for you to use. They provide a mixture of pre-recorded lectures, presentations, and practicals from the course, and will give you a snapshot of what to expect in the 2025 edition.
Flash talks
All participants will be asked to give a short presentation about their research work as part of the course. These provide an opportunity to share their research with the other participants and provide a forum for discussion. Successful applicants will be required to submit their talks upon registration.