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The NEXTFLEX® Lysosomal Storage Disorders NGS Hybridization Panel simplifies the identification of relevant SNVs, indels, and CNVs in 11 genes that have been associated with LSD.
The NEXTFLEX® Targeted NGS Hybridization Panel 1 simplifies the identification of relevant SNVs, indels, and CNVs in more than 75 genes related to endocrine and metabolic disorders, hemoglobinopathies, and primary immunodeficiencies.
The NEXTFLEX® Small RNA-Seq Kit v3 with UDIs uses patented and patent-pending technology to provide a reduced-bias small RNA library preparation solution with Unique Dual Indexes (UDIs) for Illumina® sequencing. PerkinElmer's approach to reducing ligation-associated bias involves the use of adapters with randomized bases at the ligation junctions, resulting in greatly decreased bias in comparison to standard protocols.
To simplify your DNA sequencing, we offer affordable bundles containing NEXTFLEX® Rapid DNA-Seq library prep reagents and NEXTFLEX DNA Barcodes.
NEXTFLEX-HT™ Barcodes are single-index adapters for Illumina® sequencing providing flexibility and high-throughput capabilities in sequencing applications.
The NEXTFLEX® Targeted NGS Hybridization Panel 2 simplifies the identification of relevant SNVs, indels, and CNVs in more than 65 genes related to amino acid disorders, fatty acid disorders and organic acid disorders.
The NEXTFLEX® Cystic Fibrosis Amplicon Panel allows you to quickly target and sequence 28 exons of the CFTR locus.
NEXTFLEX-96™ DNA barcodes are compatible with Illumina® sequencing and provide flexibility and high-throughput capabilities in sequencing applications.
NEXTFLEX® tRNA/YRNA blockers seamlessly integrate into the library prep to block the formation of tRNA and YRNA products in your small RNA libraries when used with the NEXTFLEX Small RNA-seq Kit v3.
The NEXTFLEX® Duchenne Muscular Dystrophy (DMD) NGS Hybridization Panel (RUO) simplifies the identification of relevant SNVs, indels, and CNVs in the dystrophin gene associated with DMD.
The NEXTFLEX® Core Exome NGS Panel simplifies the identification of relevant SNVs, indels, and CNVs in ~6,000 genes associated with common genetic disorders.
The NEXTFLEX® Unique Dual Index Barcodes are barcoded adapters, for sequencing on Illumina® sequencers, providing data security in sequencing applications.
NEXTFLEX® DNA barcodes are single indexed adapters for Illumina® sequencing that provide flexibility and high-throughput capabilities in sequencing applications.