Targeted sequencing of forensically relevant STR and SNP loci empowers you to generate leads, even on cold cases. With NGS, crime laboratories can address hundreds of markers in a single test. This lets labs develop a more thorough, detailed profile from degraded, mixed, and limited DNA samples.
See how researchers are using next-generation sequencing on the MiSeq FGx to maximize the chances for a useful profile in criminal casework.
9 hours/90 minutes hands-on
Access a wider range of informative SNPs with a single kit. Includes allreagents to prepare sequencing libraries from forensic DNA samples.
30 hours/30 minutes hands-on
Pre-filled, ready-to-use reagent cartridges, specifically designed for the MiSeq FGx System.
1 hour
This fully validated software can be used to manage, analyze and interpret a wide range of forensics casework and database samples.
Millions of DNA profiles are curated in national DNA databases. NGS can help labs produce high-quality forensic DNA profiles more efficiently. Because Illumina sequencing technology analyzes multiple marker sets simultaneously, rather than sequentially, there is a faster turnaround.
See how criminalists are performing next-generation sequencing on the MiSeq FGx to build high-quality forensic DNA databases.
9 hours/90 minutes hands-on
Access a wider range of informative SNPs with a single kit. Includes all reagents to prepare sequencing libraries from forensic DNA samples.
30 hours/30 minutes hands-on
Pre-filled, ready-to-use reagent cartridges, specifically designed for the MiSeq FGx System.
1 hour
This fully validated software can be used to manage, analyze and interpret a wide range of forensics casework and database samples.
Illumina SBS offers a massively parallel approach for sequencing forensic PCR amplicons, both nuclear and mitochondrial. NGS enables scientists to utilize a single platform and optimal workflow to overcome the widest range of difficult samples often encountered in missing persons cases. Perform mitochondrial sequencing using the Research mode on the MiSeq FGx instrument.
See how other forensic scientists are using a massively parallel approach on the MiSeq FGx to identify unknown remains.
1.5 hours/15minutes hands-on
Prepare sequencing-ready libraries for small genomes like mitochondrial DNA in less than 90 minutes.
30 hours/30 minutes hands-on
Pre-filled, ready-to-use reagent cartridges, for running the MiSeq FGx System in Research mode. Use for sequencing mtDNA libraries.
1 hour
Enables streamlined variant analysis of d-loop and whole mitochondrial DNA sequence data.
Enables simplified visualization of d-loop and whole mitochondrial DNA sequence data.

In Research mode on the MiSeq FGx System, you can access any application or method that can be done on the MiSeq System. Perform targeted gene, small genome, and amplicon sequencing, as well as 16S metagenomics and targeted gene expression analysis.
See All MiSeq Research Applications