Genomic Analysis is the Cornerstone of Personalized Medicine
The genetic code holds the key to achieving authentic personalized medical care. Achieving an in-depth understanding of the complex interactions between our genome, the environment, and lifestyle factors will allow clinicians to provide medical services which are more effectively targeted toward health promotion and preventive management of hereditary diseases.
Conditions such as Alzheimer’s disease, ischemic heart disease, diabetes mellitus, and cancer all have a strong hereditary component and are among the top causes of morbidity and mortality all over the world. The application of Next-Generation Sequencing technology provides timely, concise, and accurate genetic analyses of variants. Coupled with our innovative AI models, this data is presented as clinically-oriented, intervention-focused, and data-driven information that aids clinicians in critical decision-making.
The Beauty of Our Revolutionary
Genomic Analysis Technology
Genomic analysis has failed to gain widespread acceptance in routine clinical practice for several reasons. Some significant challenges include the enormous computational complexity of genomic interpretation, its perceived lack of actionable application by physicians, and the technological hurdles plaguing the industry such as sample contamination, experimental noise, unclear sequencing variations, and the unknown clinical significance of many newly recognized variants.
Our unique approach to these challenges involves the integration of several classes of interconnected, yet distinct revolutionary solutions.
Next generation sequencing
Next-Generation Sequencing technology is a parallel processing technology that offers high-throughput genomic analyses. This allows physicians to sequence entire genomes quickly and accurately with little room for error. It offers significant scalability, comprehensive genomic coverage, faster turnaround time, and a significantly lower limit for variant detection. The innovative combination of Next-Gen sequencing and AI technologies also allows for greater flexibility and the ability to adapt to evolving technology.
Unique machine learning AI
Our unique Machine Learning AI makes use of an efficiently programmed algorithm to detect, annotate and classify multiple types of genetic variants. This technology also offers end-to-end workflow analysis from library preparation to gene code sequencing and finally data analysis. The advantage of our system is that this information is presented to clinicians as clinically-relevant data-driven information that can aid you in the diagnosis, disease prevention, and management of numerous hereditary conditions.
Software As A Service (Saas)
The Clinical Shift is built on a Software as a Service (SaaS) framework. This model allows our users greater flexibility and secured access to our services anywhere in the world as long as they have a functioning internet connection. We offer a wide range of databases for more effective analysis, customizable filtering options, and a user-friendly interface to aid in genomic interpretation. Also, as expected of any medical service, complete data security and patient information confidentiality is assured.
Constantly Evolving
Knowledge and Services
The world of genomic analyses is a constantly evolving field. The discovery of new sequencing technologies and variants brings us ever closer to understanding the true nature of our genetic code. Therefore at ANM Software we are constantly at the forefront of research and development geared towards improving our existing services and discovering new ways to tackle the challenges of clinically-oriented variant detection and analysis.
