Malte Borggrewe’s Post

Single-cell mRNA sequencing is everywhere. But what’s important to know for biologists? (Part 1) When I started my computational biology journey, the first set of data I got was scRNA-seq, and I was immediately fascinated by the technology. Below you see my first UMAP! 😊 But how do you start as a biologist without experience in bioinformatic data analysis? I will post a 5 part series on LinkedIn in the next 2 weeks, helping you to figure out what’s important and how to start. Let’s start with an overview of the technology, when to use it, when NOT to use it, and what insights you can expect to gain. 👨🔬 What is scRNA-seq? Single-cell mRNA sequencing allows us to examine the transcriptome at the individual cell level. This provides a detailed view of the gene expression landscape, revealing heterogeneity within seemingly uniform cell populations. 🗝 Key Benefits and when to use scRNA-seq: • Uncover Cellular Heterogeneity: Identify distinct cell types and states in complex tissues. • Trace Lineage and Development: Track the differentiation paths of cells during development. • Discover Rare Cell Populations: Detect low-abundance cell types that might be missed in bulk RNA-seq. 🚧 Disadvantages: • Cost and Resources: scRNA-seq can be expensive and resource-intensive. For studies requiring large sample sizes or high-throughput analysis, consider the cost-benefit ratio and other technologies (bulkRNAseq). At this moment, cost for one sample including sequencing is around 2,000€. • Technical Complexity: The method requires meticulous sample preparation and sophisticated data analysis. That’s where I want to help you with my post series. • Tip of the iceberg: With scRNA-seq, you uncover cellular heterogeneity, but only detect 2,000-3,000 genes per cell, capturing just the highly expressed transcripts. It's the tip of the iceberg compared to bulk RNA-seq, which provides all transcripts but misses cellular diversity. 🔍 Conclusion: scRNA-seq is a transformative tool with broad applications across various fields of biology and medicine. By understanding when and how to leverage this technology, researchers can gain unprecedented insights into cellular function and dynamics. However, careful consideration of the costs, technical demands, and specific research goals is crucial to maximizing the benefits of this cutting-edge technique. ⏭ Next up: Quality is key! #scRNAseq #Genomics #Research #Biotechnology #Immunology #Neuroscience #DevelopmentalBiology #SingleCell #Transcriptomics #Biotech #StartUps #Academia

  • https://doi.org/10.1126/science.aba5906

Malte Borggrewe I was doing ScRNA seq analysis from the pre exisiting data taken from 10X genomics ,Intitial analysis went well around 50% was done but when i went on to proceed with the Data scaling part it showed errors and even now i cant find the issue maybe because my system doesnt supports it .I was using Rstudio via seurat workflow

Like
Reply

Just started my Phd , and have plans of doing scRNA-seq but have minimum knowledge of coding and computational biology. Hoping to learn a lot from you and eagerly waiting for other parts , also if you can tell from where to learn all these things then it will be very much helpful.

Great start to your series! scRNA-seq is invaluable in cancer research for exploring the tumor microenvironment and in developmental biology for tracing cell lineage. In contrast, bulk RNA-seq is ideal for examining broader transcriptomic trends in studies where detailed cellular resolution is less critical, like observing treatment responses, namely, TREATMENT vs NO TREATMENT experiments. Your insights are opening up vital discussions on the strategic use of these technologies!

I’ve been looking for exactly this kind of learning journey documentation. Following.

For someone starting out in Computational Biology and Bioinformatics, what will you advise he start with, bulkRNASeq or ScRNASeq? I was asked this question during a talk. What would be your best answer and why?

Like
Reply

I will start my first single-cell RNA-seq project soon; thanks for the introduction. I am looking forward to the quality control part 🙂

thank you so much my 1st project in bioinformatics is analyzing scRNA-seq data and it's quite challenging as a pure biologist without prior experience in bioinformatics.. looking forward for more

Like
Reply

Iam a biologist fresh graduate student I want to begin this road , can you tell me from where can i start

Like
Reply

Wouldn't a 3rd UMAP axis be beneficial to separate clusters 1-4?

Like
Reply

Malte Borggrewe Thanks for the very useful summary!

Like
Reply
See more comments

To view or add a comment, sign in

Explore content categories