Sophia Genetics

Q: Where is Sophia Genetics headquartered?

Sophia Genetics is headquartered in Saint-Sulpice, Switzerland, a small town just outside of the bustling city of Lausanne. The company was founded in 2011 and has since grown to become a global leader in data-driven medicine, with additional offices in the United States, United Kingdom, and other key locations around the world.

49 cited products 297 protocol citations

Sophia Genetics is a leading provider of innovative software solutions and advanced analytics tools for genomic research and clinical applications.
The company's flagship product, PubCompare.ai, is a comprehensive database that allows researchers to uncover citations, trends, and insights related to the use of Sophia Genetics' products across various research protocols.
By leveraging this powerful platform, scientists can efficiently identify studies that have utilized Sophia Genetics' cutting-edge equipment, consumables, reagents, and software, supporting their own scientific investigations.
Sophia Genetics' offerings span a wide range of research domains, including but not limited to genomics, bioinformatics, and molecular biology, empowering researchers to make data-driven decisions and advance their scientific discoveries.

49 products from Sophia Genetics

Alamut visual by Sophia Genetics

Cited in 29 protocols

Sourced in France, United States

Alamut Visual is a software tool designed for the visualization and analysis of genetic data. It provides a comprehensive platform for the interpretation of DNA sequence variations and their potential impact on human health.

Alamut by Sophia Genetics

Cited in 22 protocols

Sourced in France

Alamut is a software tool developed by Sophia Genetics to assist with the analysis and interpretation of genetic variants. It provides access to comprehensive databases of genetic information and supports the annotation and classification of DNA sequence variations.

Alamut software by Sophia Genetics

Cited in 20 protocols

Sourced in France

Alamut software is a bioinformatics tool used for the analysis and interpretation of genetic variants. It provides a comprehensive database of genomic information, including gene annotations, disease associations, and population frequency data. The software is designed to assist in the identification and assessment of genetic variations, supporting healthcare professionals in the diagnosis and management of genetic disorders.

Alamut visual version 2 by Sophia Genetics

Cited in 19 protocols

Sourced in France

Alamut Visual version 2.7 is a software application that provides a visual interface for analyzing and interpreting genetic variants. The core function of this product is to assist in the visualization and interpretation of genetic data.

Alamut visual software by Sophia Genetics

Cited in 19 protocols

Sourced in France, Switzerland

Alamut Visual is a software application developed by Sophia Genetics. It provides a comprehensive platform for the visualization and analysis of genetic data. The software's core function is to enable users to interpret and annotate genetic variants identified through various sequencing technologies.

Alamut visual v2 by Sophia Genetics

Cited in 18 protocols

Sourced in France

Alamut Visual v2.11 is a genomic visualization tool designed for the analysis and interpretation of DNA sequence data. It provides a comprehensive platform for viewing, annotating, and analyzing genetic variants within the context of genomic information.

Alamut visual 2 by Sophia Genetics

Cited in 13 protocols

Sourced in France

Alamut Visual 2.7.1 is a software application designed for the visualization and analysis of genomic data. It provides a user-friendly interface for displaying and interpreting genetic sequences, variants, and annotations.

Alamut batch by Sophia Genetics

Cited in 12 protocols

Sourced in France

Alamut Batch is a software tool for the analysis and annotation of genomic variants. It provides a comprehensive set of functionalities for the interpretation and reporting of genetic variations detected in DNA sequencing data.

Sophia ddm software by Sophia Genetics

Cited in 11 protocols

Sourced in Switzerland, United States

Sophia DDM software is a digital data management solution designed for genetic laboratories. It provides a secure platform for storing, analyzing, and sharing genomic data.

Alamut 2 by Sophia Genetics

Cited in 9 protocols

Sourced in United States, France, Switzerland

Alamut 2.0 is a software tool designed for the analysis and interpretation of genetic variants. It provides a comprehensive platform for visualizing and annotating genetic data, including support for various file formats and integration with external databases.

Company FAQ

Where is Sophia Genetics headquartered?

What types of equipment and research fields does Sophia Genetics typically work with?

Sophia Genetics' technology is commonly used in a wide range of medical and life sciences research fields, including oncology, rare diseases, and reproductive health. The company's platform is compatible with a variety of next-generation sequencing (NGS) platforms and can analyze data from DNA, RNA, and even proteomics experiments. This versatility allows researchers to leverage Sophia's powerful analytics tools across a diverse array of applications.

How can PubCompare.ai help researchers find relevant protocols for their work?

PubCompare.ai is a unique tool developed by Sophia Genetics that helps researchers quickly identify experimental protocols that are a good match for the specific products and equipment they are using. By searching a comprehensive database of published methods, PubCompare.ai can suggest protocols that are likely to be compatible, saving time and reducing the risk of experimental errors or wasteage. This hniques to improve the overall reproducibility and efficiency of their research.

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About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

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