A new single-cell study has found that aneuploidy is common in early-stage human embryos, a finding that may have implications […]
*** This post was written by Dr. Anja Brunner, science writer (Science Inbound) Interview with Cristina Gamba, Global Product Manager […]
A study from the Murdoch Children’s Research Institute (MCRI) has found a genetic cause for a rare disease that causes […]
Front Line Genomics is delighted to announce the launch of D4 Global: the world’s first truly global event focusing on […]
The human body has 40 trillion cells and roughly 200 different cell types. Amongst the diverse cell types lies incredible […]
Tackling Disease-Related Repeat Expansion Analysis – Marzia Rossato What is the Dark Genome? The dark genome refers to parts of […]
Binx Health and Sherlock Biosciences have announced a partnership to develop the world’s first point-of-care diagnostic test for COVID-19 using […]
Sequenced genomes retain a surprisingly large number of “dark” regions – sections that have proven difficult to characterise via short-read […]
Single nucleotide variants (SNVs) are implicated in about half of all genetic diseases and so, accurately targeting and editing these […]
A new single-cell analysis study of airway samples of COVID-19 patients has found that drugs targeting chemokine receptors may be […]
