Those workshops are intended for wet lab scientists who would like to learn about bioinformatics. They are held online on 1:1 or in small groups on flexible dates.
Topics/levels can be adapted, depending on your need. Please contact me for any R / NGS data analysis workshop request.
Get comfortable using R and RStudio while analysing a dataset, from start to finish.
Learn how to get started with R, load libraries, read in tabular data, generate and modify R objects, manipulate datasets and visualize the results with ggplot.
Is this workshop for you?
This workshop is intended for researchers/PhD students in biosciences who are not comfortable using R to analyse their own data. You will learn the bascis needed to start with data analysis, including NGS. There is no prerequisites in R or genomics.
Program: (three ~2-hour sessions on three consecutive days)
Next available session: May 2025
from 10 am to ~12.15 pm (GMT+2 Central Europe)
from 12 pm to ~2.15 pm (GMT+3 Arabia Standard Time)
from 5 pm to ~7.15 pm (GMT+8 Singapore)
Improve your R scripts:
use conditional statements (perform different actions based on different conditions)
implement your own functions (reuse code that performs a specific task)
efficiently manipulate vectors (repetitively perform an action without using loops)
customize your plots (advanced ggplot2)
more on request
Next available session: On demand
Learn how to generate professional and interactive html reports using R:
Next available session: On demand
Implement your own Shiny app, and allow your collaborators to explore and visualize your datasets easily.
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.comWhy learn command line / batch script?
Most bioinformatics tools run on Linux systems using command lines. Workflows and runs can be automated using batch scripting.
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.comMost NGS data analysis start after sequencing, with fastq files. The data are usually first analysed on Linux systems and downstream analysis can then be processed with specialised R packages.
Next available session: On demand
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.comI always appreciate student’s feedback and suggestions to improve my content.
“Thanks Clem that was super helpful” (R for beginners workshop)
“Great workshop” (R for beginners workshop)
“That’s perfect” (R for beginners workshop)
“Excellent all throughout” (R for beginners workshop)
“Keep organising follow up workshop similar to this” (R for beginners workshop)
“Keep organising and helping researchers” (R for beginners workshop)
“I feel it was run really well” (R for beginners workshop)
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.comAfter a Master in Bioinformatics obtained in 2012 (Bordeaux - France), I worked as a bioinformatics research assistant in molecular biology (ZMBH, Heidelberg - Germany) and medical research (dkfz, Heidelberg - Germany) for 4 years.
I then obtained a PhD in Applied Bioinformatics (UWA, Perth - Australia in collaboration with BASF, Ghent - Belgium), focused on NGS analysis and epigenetics, in 2021.
Since then, I work as a bioinformatician in one of the main Australian sequencing facilities. In parallel, I became a consultant in web development and started implementing web apps (in Shiny R) for a civil engineering company (Engineering Design and Certifications, Gold Coast - Australia) specialized in structural engineering.
In order to offer the best support in helping people perform their own data analysis independently, I became a Carpentries Instructor in 2023. The Carpentries Instructor Training curriculum was originally released in 2016 and is focused on evidence-based teaching practices.
I have a specific interest for data visualization and generation of user-friendly interfaces which help scientists get a clear overview of every project outcome.
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.comData visualization in R is diverse and highly customisable. Learn how generate high-quality, publishable graphics.
Some examples I made to illustrate different project, mainly using ggplot2:
Read number per sample and per project after demultiplexing, part of a html report automatically generated at the end of each sequencing run
Barplot representing the duration (walltime) of a workflow per library type
Volcano plot of differentially expressed genes, as part of a RNAseq analysis
Amount of biotypes (biological significance of genes) represented in an RNAseq sample
Representation of the homologous gene pairs distributed in collinear regions between two reference genomes
PCA analysis of methylation content of samples sequenced using different library types
Density of differentially methylated bases across promoters
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.comFor any request, please contact me at: clem@bioinfo-consult.com
Made in R by Clem M
ABN 62 778 900 494
Email: clem@bioinfo-consult.com