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Genetic variants linked to male breast cancer found

A recent study published in the Journal of the National Cancer Institute has discovered three genetic variants linked to an […]

Whole-exome sequencing as a tool to detect inborn errors of metabolism

A study published in Nature Medicine has demonstrated the potential of whole-exome sequencing (WES) in detecting inborn errors of metabolism […]

The UK Biobank releases first results from COVID-19 study

Early results analysed as part of the UK Biobank’s COVID-19 antibody study have been released. Samples that were collected from […]

Study finds expanded tandem repeats contribute to Autism Spectrum Disorder

Autism spectrum disorder (ASD) affects one in 54 children in the US and is associated with a heritability between 50-90%. […]

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 […]