Genomics

Nanopore sequencing and a self-enhancing AI model team up to enable a faster and more accurate method for reading synthetic genes.

A deep dive into the skin barrier uncovers the critical role immune cells play in structural reinforcement and wound healing.

A groundbreaking multinational atlas of the body’s frontline defenders reveals hidden variations that could enhance precision health efforts worldwide.

A new spatial multi-omics tool merges different levels of biological data from the same tissue sample to better differentiate finer details at different health states.

Scientists identify a new, distinct group of the deadly yeast Candida auris, and urge the expansion of global surveillance efforts.

A comprehensive study of liver tumours reveals that a small fraction of aggressive cells can have an outsized effect on patient outcomes.

A*STAR researchers devise a new streamlined method for analysing thousands of genes at once on a tissue-wide scale, offering a more accessible tool to study and diagnose diseases at a cellular level.

A*STAR researchers develop a new method to study RNA’s intricate folding patterns within a single cell, revealing fresh insights into how cells develop and function.

Bambu, a new computational tool for analysing genetic data, effectively identifies and quantifies complex gene patterns.

Researchers performed a comprehensive genetic sequencing of individual tumour cells to refine existing colorectal cancer classifications.

A new computational tool accurately predicts RNA modifications from sequencing data, allowing researchers to study and develop novel therapies for complex diseases such as cancer.

Researchers extract insights from large databases of genetic and clinical information in a bid to develop more robust, data-driven breast cancer screening frameworks.