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Applying Personalized Genomics to Ash Trees

At Front Line Genomics we spend a lot of time helping our audience understand and investigate the impact of genomics […]

GWAS of bipolar disorder provides new insights

A new genome-wide association study (GWAS) of over 40,000 bipolar disorder cases has provided new insights into the underlying disease […]

UK plan to deliver world-leading genomic healthcare

The UK Government has launched the latest implementation plan to deliver world-leading genomic healthcare to patients. UK Genomics As seen […]

Parental genome unification is error-prone

A new study has found that the process of combining maternal and paternal genetic information is surprisingly highly error-prone. Parental […]

Cancer cells take advantage of DNA’s 3D structure

Researchers have explored how cancer cells re-organise the 3D structure of their DNA to enhance oncogene activity. Cancer cells In […]

Single Cell Sequencing: A New Dimension in Cancer Diagnosis and Treatment

A new multi-omics approach for single cell sequencing When: May 25th at 3pm BST/ 4pm CEST/ 10 am EDT Single […]

Studying genetic changes at single-molecule resolution

Scientists at the Wellcome Sanger Institute have developed a new method – NanoSeq – that enables them to study genetic […]

Genomics in Drug Discovery & Development

Despite an increase in investment into R&D from biopharma companies, only 5-10% of drugs that enter early-stage clinical trials ever […]

1 in 6 colorectal cancer patients have hereditary gene mutation

Researchers within the Mayo Clinic Center for Individualized Medicine have found that 1 in 6 patients with colorectal cancer have […]

BioMe used to Identify new Subpopulations and Disease Risks

Accurately understanding populations and associated disease risks is important to direct resources and treatments effectively. By understanding where someone comes […]