SEQNEXT is a powerful and user-friendly application for mapping, alignment and variant detection of Next Generation Sequencing data. SEQNEXT can analyse data from all common sequencing platforms and kits (PCR-based, enrichment, sequence capture). Visualisation of all detected variants like deletions, insertions and indels of any length, SNPs, repeat regions as well as CNVs and gene fusions is clear and intuitive.
SEQNEXT offers access to public SNP-databases like dbSNP, 1000 Genomes, ClinVar, ExAC and gnomAD for classification and filtering. All result data can be exchanged with our variant database for Shared Experience And Knowledge - varSEAK, transferred to laboratory internal LIM Systems and / or issued as personalised patient reports.
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