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Blog

Announcements

Sano Genetics Deploys CloudOS to Deliver Free Genotype Imputation

By democratising access to data securely, Lifebit and Sano empower data-driven insights for DTC customers and life sciences researchers with their innovative […]

VangelisJanuary 9, 20204 min read
Technology

How to Enable a Genomic Revolution Without a Data Privacy Catastrophe

Data security and compliance are recurring themes in the many conversations I have with researchers and organisations in life sciences. This isn’t […]

VangelisDecember 19, 20195 min read
Industry

Reviving Genomics Progress: Overcoming Big Data Challenges

I have had the opportunity to get to know a great many people in life sciences. Whether pharmaceutical, biotechnology, or direct-to-consumer (DTC) […]

VangelisNovember 26, 20195 min read
Technology

CloudOS Meets Jupyter: Fixing Reproducibility Crisis in Science

Anyone working in a data-driven industry will undoubtedly recognise the name Jupyter, a clever acronym for Julia, Python and R (although dozens of other programming languages are […]

VangelisNovember 20, 20196 min read
Announcements

Lifebit and Medley Genomics Partner to Deliver Solution for New Diagnostic & Therapeutic Discoveries

Researchers can now tap new disease discoveries using Medley Genomics HotNet2 at enterprise scale, over any system, across distributed data with Lifebit […]

VangelisNovember 14, 20194 min read
Announcements

Lifebit Announces Release of CloudOS, Offering Genomic Data Federation

Lifebit CloudOS operates as a managed informatics platform that removes the industry barrier of vast amounts of inaccessible distributed omics data, enables […]

VangelisNovember 7, 20192 min read
Industry

HotNet2 Algorithm: Detecting Cancer Genes & Disease with Precision

Why study cancer heterogeneity? Introducing HotNet2, a cancer gene detection algorithm, to support your efforts. Understanding a cancer gene detection algorithm is […]

VangelisNovember 4, 20198 min read
Industry

Finding Genetic Variations Associated to Complex Diseases: Needle in Haystack

There are 3,000,000,000 base pairs in the human genome, which define our individual code. 99% of these are identical for all humans- […]

VangelisOctober 16, 20199 min read
Technology

How-To Guide: Standardised Secondary Genomics Analysis with Illumina’s DRAGEN

The quest for robust, rapid, scalable & integrated genomics analysis In today’s world of bioinformatics, data has gotten too broad and complicated, […]

VangelisSeptember 20, 20195 min read
Technology

Genome Browser: Analysing Genomic Data Without Bioinformatics Skills

As sequencing technologies become more performant year over year, three challenges for the research community arise: 1) astronomical quantities of data are […]

VangelisSeptember 13, 20194 min read
Technology

How to Run nf-core Analysis on the Cloud Using nf-core/rnaseq Pipeline

nf-core is a great community-driven effort which makes bioinformatics pipelines very standardised and incredibly simple to run (Ewels et al., 2019) (check out our previous […]

VangelisAugust 9, 20195 min read
Technology

CloudOS Meets nf-core: Standardising Cloud-Native Bioinformatics Pipelines

Bioinformaticians in the pursuit of best practices The democratisation of Next Generation Sequencing technologies has made omics data more available than ever […]

VangelisAugust 7, 20195 min read
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