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Insights from Largest-Ever Tumour Genome Analysis Ready for Clinical Use

Written by Charlotte Harrison, Science Writer  A study headed by Cambridge University scientists has conducted the largest whole-genome sequencing analysis […]

Advancing clinical interpretation from single cell sequencing datasets – Webinar

Novel tools for data analysis and clinical interpretation The clinical translation of single cell analysis approaches into routine practice represents […]

Genome Giants – Janina Jeff, Staff Bioinformatics Scientist, Illumina

Janina Jeff is an American geneticist and Staff Bioinformatics Scientist at Illumina. Jeff is particularly interested in identifying genetic variants […]

Whole genome, whole exome or panel sequencing in precision oncology clinical trials

With a wealth of genomic technologies rapidly advancing with falling cost, implementing genomics into trials and routine care is becoming […]

The disadvantages to integrating genomics into clinical trials

Last week, we wrote a blog post on the benefits of integrating genomics into clinical trials, such as improved methods […]

Single Cell ONLINE – A virtual series

The human body has 40 trillion cells and roughly 200 different cell types. Amongst the diverse cell types lies incredible […]

FoG 2020 Presentation Andy Brass, University of Manchester: Reshaping Health: Digital futures and reality

Andy Brass is Professor of Bioinformatics at the University of Manchester. He has worked closely with Health Education England and […]

Bringing choice to sequencing – DNBSEQ technology and the HotMPS sequencing chemistry*

Next Generation Sequencing (NGS) has become a powerful tool to decipher the genetic code. It is often seen as having […]

World of Genomics: Ireland

Ireland, known in Irish as Éire, is famous for its rich heritage, traditions, Guinness, pubs and St. Patrick’s Day. Ireland […]

World of Genomics: South Korea

Famous for kimchi, K-pop and Samsung, we travel to South Korea for the latest in our World of Genomics series. […]