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Read about our latest news, updates, top-notch science, and learn more about the ins and outs of single-cell sequencing.

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Why Every Single-Cell Experiment Needs a Pilot

Single-cell sequencing has never been easier to run and never easier to misinterpret. Today, you can pick a platform, send samples, and receive a dataset with thousands of cells and…

A recent photo of PERSIST-SEQ CONSORTIUM members

Single-cell spatial transcriptomics pinpoints drug-tolerant niches in colorectal-cancer liver metastasis

In this case study, we describe our collaboration with the Colorectal Cancer Laboratory at IRB Barcelona. Through our end-to-end spatial workflow service built around Visium HD technology, we supported the identification of distinct micro-niches of colorectal cancer cells that persist after FOLFOX chemotherapy. Together, these insights provide a roadmap for developing more effective combination therapies.

Chromosomes ideogram of the human reference genome assembly GRCh38/hg38. Characteristic bands patterns are displayed in black, grey and white, while the gaps and partially assembled regions are displayed in blue and rose, respectively. Reference: Genome Data Viewer of the NCBI

Reference genomes in transcriptomic data

You have finally received your sequencing data and can’t wait to start analyzing it! But here’s the catch: raw FASTQ files alone won’t get you far. To extract meaningful biological…

Pablo Gómez Sacristán - JUNIOR BIOINFORMATICIAN

Why should you clean up your FASTQ files?

You have received a few tens or hundreds of gigabytes of sequencing data in the form of FASTQ files. If you are not yet familiar with this format, the amount of data can feel overwhelming at first. What do you do with these…

Your daily scRNA-seq data tasks: Tips-and-Tricks

Single-cell RNA sequencing (scRNA-seq) data analysis is not just pressing one button. To get from raw FASTQ files to exploratory reports or publication-ready plots, you will need to: Preprocess your…