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Run diverse Sanger sequencing and fragment analysis applications with the SeqStudio Genetic Analyzer

Designed for use by research assistants and scientists, the Applied Biosystems SeqStudio Genetic Analyzer is a low-throughput, easy-to-use, convenient benchtop system. With minimal hands-on time due to an all-in-one cartridge, the SeqStudio analyzer helps make running capillary electrophoresis (CE) experiments easier and faster. It also facilitates collaboration through Thermo Fisher Scientific's Connect cloud–based sharing and applications, and introduces new opportunities to run both sequencing and fragment analysis samples at one time.

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 Copy number determination with Multiplex ligation–dependent probe amplification (MLPA)
 Detection of low-level somatic mutations in FFPE samples using Sanger sequencing
 MethylSeq Direct workflow: a fast method for DNA methylation analysis
 
 Authenticating human cell lines using STR kits and the CE platforms
 Matching identities of iPSCs and donors using STR profiling kits
 
 Genetic analysis tools for genome editing workflows
 Using Sanger sequencing to facilitate CRISPR and TALEN-mediated genome editing workflows
 
 Detection of RNA from SARS-CoV-2 using fragment analysis
 Multiplexed target fragment analysis for detection of viral pathogens, including SARS-CoV-2
 
 A fast method for microbial identification by Sanger sequencing of the 16S rRNA gene with analysis using Applied Biosystems™ MicrobeBridge™ software
 A fast method for microbial identification by Sanger sequencing of the 16S rRNA gene with analysis using SmartGene™ web application service
 
 Simplified analysis of triplet repeat expansions with capillary electrophoresis
 Copy number determination with Multiplex ligation–dependent probe amplification (MLPA)

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