Resources
The latest in omics research, from discovery and multi-omics approaches through to diagnostics development
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Top R&D Stories of 2023
Through captivating articles, insight pieces, and spotlight interviews, we delve into the remarkable innovations, breakthroughs, and scientific marvels that have defined the landscape of research over the past year.
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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