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Comprehensive panel detects single-nucleotide variants (SNVs), amplifications, and fusions that contribute to solid tumor progression.
Perform transcriptome profiling for hundreds to tens of thousands of single cells in one experiment.
Scalable throughput and flexibility for virtually any genome, sequencing method, and scale of project.
A fast, integrated workflow for a wide range of applications, from human whole-genome sequencing to amplicons, plasmids, and microbial species.
Learn how Illumina next-generation sequencing (NGS) works, and how it's furthering forensic science.
Find out how deep mitochondrial DNA (mtDNA) sequencing is being used to identify skeletal remains.
Fast library prep delivers quality de novo assembly of small genomes.
Instructions for human mtDNA D-loop hypervariable region sample preparation.
Instructions for human mtDNA genome sample preparation.
Improved human mtDNA analysis using NGS and cloud-based computing and storage.
Researchers use NGS to obtain more information-rich data and answer more complex forensic questions.
Criminalists use MiSeq FGx for high-resolution DNA profiling to build better forensic DNA databases.
Researchers identify genetic variants that influence facial features to enable facial imaging from DNA.
Learn about the advantages of targeted NGS and view the data validating the MiSeq FGx System in this Forensic Magazine article.
Learn about the potential of NGS to solve cold missing persons cases and identify unknown human remains.
In forensic work, the smallest detail can make the difference in solving a crime.
Hear from experts in the field how massively parallel sequencing (MPS) is paving the way ahead, and why now is the time to adopt it.
Learn how the Illumina forensic genomics workflow can transform forensic applications.
Dr. Mitch Holland of Penn State explains how NGS is helping us realize the power of mtDNA heteroplasmy.
The MiSeq FGx System is the first fully validated NGS solution designed exclusively for forensic science.
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