Resources

The latest in omics research, from discovery and multi-omics approaches through to diagnostics development

NGS & Clinical Diagnostics

Antibody-Mediated Rejection and Next-Gen Sequencing in Precision Medicine

Maintaining tolerance to a graft or organ transplant is a critical aspect of treatment for precision medicine. Antibody-mediated rejection is a serious hurdle to transplantation success, but the integration of highly selected stem cells into treatment may be a solution.
NGS & Clinical Diagnostics

Data Collection, Image Modelling, and Spatial Analysis: Quality Control for Quality Data

The potential applications of deep learning tools in preliminary studies have developed along with their complexity in the past few years. Now, they could be used to help to refine a study or programme before it takes place in order to optimise its efficiency.
NGS & Clinical Diagnostics

Next Generation Nucleic Acid Extraction for NGS: Increased Yields and More Efficient Workflows for Extraction from FFPE

On-demand seminar. Learn more about the Ionic system and a real-world case study on how the Ionic is being utilized at a leading cancer centre.
NGS & Clinical Diagnostics

Data Integration in Genomic Analysis: Computational Methods for the Integration of Spatial Metabolomics

This Commentary article explores the potential applications which arise from combining multiple modalities of information to augment the spatial resolution of data.
NGS & Clinical Diagnostics

Long and Short Read Sequencing: Revolutions in Genomics Data  

In this Discussion Group Report, we investigate some recent applications of long- and short-read sequencing technologies. Continued improvements and advancements in the field mean sequencing errors are increasingly a thing of the past, while the portability of some new units makes them ideal for work in the field.
NGS & Clinical Diagnostics

Paving the Road to Multi Omics Bioinformatics

Our May Omics Series discussion group focused on the current uses and potential of multi-omics bioinformatics.
NGS & Clinical Diagnostics

De Novo Variants: Genomic Sequencing and Problem Solving for Future Treatments

In this Commentary article, we investigate the application of new research techniques to inspecting genomic data for the presence of de novo variants - genetic alterations present for the first time in one individual as a result of a variant inherited from a parent. Used in combination with data from the 100,000 Genome Project, these techniques could reduce the time taken for patients to receive a diagnosis for rare genetic diseases.
NGS & Clinical Diagnostics

Multi-Tissue Molecular Profiling: Precision Medicine for Neurodegenerative Diseases

At NGO US: In-Person 2022, Carlos Cruchaga of the Washington School of Medicine presents on using QTL and GWAS data to unlock the future of therapeutic treatment for neurodegenerative disease.

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