SeqOne germVar AI-enhanced Whole Genome Long Read variant interpretation

SeqOne’s germVar offers precise and comprehensive variant analysis tailored for long reads (RUO):

Phasing display for Compound Heterozygotes ID
Compatible with Epi2ME
Single/family cases
CNV, SNPs, INDEL, SV, STR
Advanced and intuitive interpretation hub (in-silico panels, advanced viewers, etc.)

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Ready for the challenge of WGS variant interpretation at scale with Seqone DiagAi assisting you with ranking, shortlisting, and suggesting pathogenic variants.

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Download germVar datasheet

SeqOne Genomic analysis platform

Secure. Scalable. Proven.

Used in Routine by 1000+ users in multiple very high-volume labs
Free trial testing, transparent usage-based pricing (‘fee per analysis’)
Unlimited user accounts and secured cloud health data storage at no additional costs.
International Customer Support and Application Specialists.
Automated data workflow from Sequencer (upload, analysis, exports) with SeqOne Data Sync
Compliant with data privacy and requirements with ISO/IEC 27001:2013 certifications and guaranteed data residency