Commentary

Analyzing a person’s gene expression requires mapping their RNA landscape to a standard reference to gain insight into the degree to which...

Researchers published a groundbreaking study demonstrating the reliability of combining next-generation sequencing and artificial intelligence to accurately diagnose subtypes of blood cancers and...

Long-read sequencing powers a more complete reading of genomic information. Long-read sequencing is enabling in reading genomes, transcriptomes and epigenomes in humans and other species. For its momentous methodological...

Our DNA contains four types of molecules, adenine, cytosine, thymine, and guanine—called nucleotides or bases—running along the strands that make up our chromosomes. Since there are only four, it is not unusual to find a short sequence of DNA repeating ...

$10M grant will support collaborations across the hospital to create a curated pediatric ‘cell atlas’ to identify disease origins and effective treatments...

Do we simply ingest a diagnostic probiotic based on programmed ribonucleic acids to analyze the intestinal health from individual cells in the future?

A Michigan Medicine study has identified a new potential target for treating osteoarthritis – a debilitating joint disease that affects over 31M...

Single-cell RNA sequencing (scRNA-seq) has become the most established and widely used technique within single-cell analysis. Spatial transcriptomics...

Rare cell types can have an undue influence on human health. Previous research has suggested that a subset of astrocytes—star-shaped cells in the brain and spinal cord—may be responsible for multiple...

New study uses postmortem brain tissues to understand genomic differences in individuals with attention deficit hyperactivity disorder. Researchers at the National Institutes of Health have...