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Variants in ACE2 and TMPRSS2 may explain genetic susceptibility towards COVID-19

The current COVID-19 pandemic has revealed that increased age and the presence of co-existing health conditions, such as cancer, cardiovascular, […]

Biologically-validated AI is how scientists are realising the full potential of single-cell RNA sequencing

The promise of single-cell gene expression data Genomic data are an excellent source of novel disease biomarkers and targets. In […]

Simple and powerful target enrichment method seeks cool new applications. Apply now.

*** This post was written by Dr. Anja Brunner, science writer (Science Inbound) Interview with Cristina Gamba, Global Product Manager […]

Genetic risk for Alzheimer’s progression differs with sex

It is well documented that the genetic risk for Alzheimer’s has a sex bias. Sex bias in Alzheimer’s Carrying a […]

Single-cell copy number profiling unveils the genetic diversity of cancer

The genetic information of a cancerous tumour is typically obtained by sequencing the tumour cells together, rather than analysing them […]

Deep learning in genomics – are we there yet?

As genomic sequencing becomes more routine, handling the sheer volume of data being produced is causing major issues. We must […]

A look inside a rapid exome sequencing lab

The ability to sequence a patient’s genome can be an invaluable tool in healthcare, especially as we move towards more […]

Günther Brueggenwerth and Arndt Schmitz from Bayer tell us about Radiomics

We caught up with Günther Brueggenwerth and Arndt Schmitz from Bayer at the Festival of Genomics in January to talk […]

Reverse genetics allows mapping of SARS-CoV-2 in the body

A new study accepted by Cell showed that SARS-CoV-2 infects the nasal cavity to the greatest degree and infects and […]

The UK is developing a new approach to patient-centric precision medicine research

Sano Genetics, Zetta Genomics and Genomics England have partnered to develop a novel system to allow rare disease patients and […]