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TISCH: a tumour microenvironment single-cell transcriptomic database

Researchers at Tongji University, Shanghai, have developed a large-scale curated database that integrates tumour microenvironment (TME) single-cell transcriptomic data, known […]

scREAD: single-cell RNA-Seq database for Alzheimer’s Disease

Researchers at The Ohio State University have developed an integrated database known as scREAD – single-cell RNA-Seq database for Alzheimer’s […]

Should We Sequence all Genomes at Birth and Make a National Database?

Some genetic variants only have weak associations with specific conditions or traits, making it difficult to predict how a child […]

Interpreting genetic variants in type 2 diabetes

Numerous genetic variants in the human genome have been linked to type 2 diabetes. However, as most of these variants […]

Genomics week in brief: Week ending 9th October

Check out the latest Genomics Week in Brief, jam-packed with some of the most recent genomics news and research. Top […]

Studying cancer through the lens of protein-protein interactions

Researchers at the Cancer Cell Map Initiative have explored hundreds of previously unknown protein-protein interactions suspected to drive cancer. Their […]

The rollercoaster ride of gene therapy (admission fees required)

Where there is a symptom there is hopefully a treatment. For example, if I have a headache, I reach straight […]

A Spotlight On: Data Sharing – Mahsa Shabani

Mahsa Shabani is an Assistant Professor in Privacy Law at the Faculty of Law and Criminology, Ghent University in Belgium. […]

Cancer Genomics Projects: The Collection

The cancer genome has been sequenced for more than a decade. This has created an abundance of relevant information that […]

Cancer Genomics: From Diagnosis to Treatment

Introduction The first publication of cancer genome sequencing was in 2006, whereby more than 13,000 genes involved in breast and […]