Findacure Annual Conference: Repurposing Drugs for Rare Diseases
Around 80 delegates joined Findacure for their Annual Conference at the Royal College of Nursing in London. These are always fascinating meetings (which is […]
Festival of Genomics 2019
The Festival of Genomics 2019 has moved from the cavernous Excel stadium to the more intimate environment of the Business Development Centre […]
Webinar: How to Implement & Run Google DeepVariant
In this webinar, Lifebit co-founder and Chief Technological Officer, Dr. Pablo Prieto, and Lifebit Bioinformatician Phil Palmer explore Google DeepVariant and show how this variant calling […]
Top 4 Highlights from Biodata World Congress 2018
This year the BioData World Congress held in Basel, Switzerland was the largest meeting to date, with a wide range of attendees […]
Webinar: Re-Analyse RNA-Seq Public Data From SRA
RNA-seq reanalysis from SRA is now faster and more accessible thanks to Lifebit CloudOS. In this webinar recap, we guide you through […]
Frontlines of Rare Disease Diagnoses: Interview with Genomics England’s data scientists
Rare disease diagnosis genomics is undergoing a revolution. Genomics England’s initiatives, supported by Lifebit, are enabling faster, more accurate diagnoses. We spoke […]
Nextflow Tutorial: Developing nf-core DeepVariant, a Google Variant Caller
This Nextflow DeepVariant tutorial is designed for bioinformaticians looking to create reproducible pipelines. If you are a bioinformatician with a bit of […]
Scaling Reproducible Genomics Analyses for Clinical Environments: The Next Frontier in Healthcare
A bit of background Scaling genomics in clinical environments is key to modernizing healthcare. Lifebit’s platform enables this with privacy-first infrastructure. Much […]
Metagenomic Data Analysis on Steroids: Insights from Dr. Martin Steinegger
Preface Our new series entitled “Bioinformatics Superheroes”, aims to focus the spotlight on researchers that have heavily contributed to the field of […]
nf-core: Standardising Nextflow Pipelines through Community-Driven Initiative
Genomics research is creating a big (data) problem nf-core Nextflow pipelines are driving standardization in genomic workflows. It’s no secret that the […]