Most genetic alterations linked to disease aren’t in genes but are in the ‘dark genome’. Nucleome is using new technology to shine a light in these unknown depths and find the hidden genetic connections to disease.
All in Women in genetics
Most genetic alterations linked to disease aren’t in genes but are in the ‘dark genome’. Nucleome is using new technology to shine a light in these unknown depths and find the hidden genetic connections to disease.
UK Biobank has made half a million whole genome sequences available for research - so what can we learn from them?
Professor Carrie Partch is researching what happens when circadian rhythm genes go wrong and whether we can create drugs for jet lag.
We chat with Dr Priya Crosby who is interested in how circadian rhythms work at the cellular level, and how molecules can tell the time.
Caroline Dean has devoted her research career to understanding how plants sense and respond to the changing of the seasons.
Matthew Cobb, science author and Professor of Zoology at the University of Manchester, has been re-evaluating the role of Rosalind Franklin in the discovery of the structure of DNA.
Cordelia Langford is the Director of Scientific Operations at the Wellcome Sanger Institute. Her career has spanned the early days of DNA sequencing to the Human Genome Project and today’s industrial-scale genomic pipelines.
At the beginning of 2020, UCL group leader Lucy van Dorp set to work using her genetic analysis skills to track the SARS-CoV-2 virus as it spread and mutated in animals as well as humans, providing vital insights to help us understand and tackle the pandemic.
Cecilia Lindgren is Professor of Genomic Endocrinology & Metabolism at the University of Oxford, and director of the Big Data Institute. She’s dedicated her career to understanding why and how people become overweight and obese, and how we can help them.
Dr Rosa Cheesman from the University of Oslo explains how genetics can help us understand complex human traits and behaviours such as education
Growing cells in the lab isn’t as easy as you might think. We explore the story of how Henrietta Lacks’s immortal cells (known today as HeLa cells) became the go-to human cell line for biomedical research, and the impact they’ve had as a result.
We explore the life and work of Hilde Mangold, whose work in developmental genetics led to the discovery of the Spemann-Mangold organiser.
We explore the life of Salome Gluecksohn, a woman and a Jew in early 20th century Germany whose experiments with mice sparked a new field in science: developmental genetics.
We discover how a chance encounter with some white-gloved mice led to new insights into heredity, through transgenerational epigenetic inheritance.
A chance encounter between a seamstress and a scientist starts a 25-year long crusade to understand the nature of hereditary cancer.
Maud Slye was one of the first people to investigate how cancer susceptibility could be inherited, with the help of 150,000 mice.
The diversity and success of life on this planet may be the result of cells buddying up and moving in together, combining their resources to create new organisms with advantageous new skills.
The story of the discovery of RNA splicing needs a re-edit.
Just as aglets stop our shoelaces from fraying, telomeres do the same job for our chromosomes, making them a hot topic in cancer and ageing research.
What did Watson and Crick discover? Rosalind Franklin’s notes…