This activity was supported by the National Science Foundation under Award Number 1927620. Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily ...

There are an estimated 6,000 Mendelian diseases, most of which still lack cures. Gene editing is an essential technology for studies aimed at generating data about disease-causing gene mutations and ...

Investigators at CHOP and UPenn found that lower cell counts could still be associated with poor outcomes if the cells were poorly differentiated.

New research suggests that large language models like GPT-4 could streamline the process of gene set enrichment, an approach what genes do and how they interact. Results bring science one step closer ...

I am a doctoral trainee working in Dr. Kaixiang Cao’s lab. Our lab is interested in understanding how epigenetic events, including histone modifications, DNA modifications, and nucleosome positioning, ...

Enhancer hijacking emerges as a major “missing driver” mechanism in LBCL/PCN, enabling detection of non-chimeric oncogene activation such as IGL::BCL2, IGH::CCND2, and MAFA/MAFB rearrangements.

Claudia Christowitz received funding from the National Research Foundation, South Africa. Cancer treatment is becoming more personalised. By considering a patient’s unique genetic and molecular ...

10x Genomics, Inc. (Nasdaq: TXG), a leader in single cell and spatial biology, today announced the launch of the next generation of its high-performance Flex assay, featuring automation-compatible ...

The National Academies will organize a workshop on research needs to advance functional genomics over the next 10-20 years. The workshop will draw on information and ideas from experts who will ...