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African genomes: Insights into human migration and health

Using whole-genome sequencing, researchers have explored the breadth of genomic diversity across Africa, gaining further insight into human migration and […]

Genome Editing: How to Predict and Detect Collateral Damage

A recent paper, published in Cell, discusses how to anticipate the molecular events that may arise from genome editing and […]

Genome UK: The future of healthcare

Genome UK The UK has launched its new National Genomic Healthcare Strategy, with the goal of cementing its status as […]

Understanding genetic variation: An integrated personal and population-based Egyptian genome reference

The power of the Human Genome Project was its universality: one genome to represent all humankind. The next challenge is […]

Whole-exome sequencing as a tool to detect inborn errors of metabolism

A study published in Nature Medicine has demonstrated the potential of whole-exome sequencing (WES) in detecting inborn errors of metabolism […]

Biologically-validated AI is how scientists are realising the full potential of single-cell RNA sequencing

The promise of single-cell gene expression data Genomic data are an excellent source of novel disease biomarkers and targets. In […]

100kb into the genome – a quest to improve target enrichment

*** This post was written by Dr. Anja Brunner, science writer (Science Inbound) Armed with a decade of experience in […]

A look inside a rapid exome sequencing lab

The ability to sequence a patient’s genome can be an invaluable tool in healthcare, especially as we move towards more […]

New single-cell sperm sequencing method uncovers insights into meiotic variation

A new method has allowed researchers at Harvard Medical School to examine variation in meiosis by studying tens of thousands […]

How do you achieve cheaper, faster sequencing?

* The following article is written with excerpts from the second edition of The Sequencing Buyer’s Guide. Download the latest […]