omnomicsNGS
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omnomicsNGS
Software for annotation, classification and reporting of found variants in NGS data of patients with CE mark in clinical oncology, other genetic testing, clinical research projects or together with a biobank as the repository for genomic variants. The software provides information on genomes and variants from multiple sources for the evaluation and classification of common and rare genetic disorders from NGS panels, whole genome and whole exome sequencing. You can use it as a cloud solution, but also integrate it locally or potentially within regional or national IT structures. The user organisation is provided with tools for adding information to the platform and can define its own template gene panels, biomarkers, and reporting templates. The software enables fast reporting according to the best practice guidelines of ACMG and ASCO/AMP/CAP.
For more information click here: https://euformatics.com/ongs/
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omnomicsNGS
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- Producer: Euformatics
omnomicsNGS
Software for annotation, classification and reporting of found variants in NGS data of patients with CE mark in clinical oncology, other genetic testing, clinical research projects or together with a biobank as the repository for genomic variants. The software provides information on genomes and variants from multiple sources for the evaluation and classification of common and rare genetic disorders from NGS panels, whole genome and whole exome sequencing. You can use it as a cloud solution, but also integrate it locally or potentially within regional or national IT structures. The user organisation is provided with tools for adding information to the platform and can define its own template gene panels, biomarkers, and reporting templates. The software enables fast reporting according to the best practice guidelines of ACMG and ASCO/AMP/CAP.
For more information click here: https://euformatics.com/ongs/
- Producer: Euformatics
omnomicsNGS
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