Oxford Gene Technology - SureSeq myPanel™ NGS custom FH panel
Manufactured by Oxford Gene Technology
Choose your perfect Familial Hypercholesterolemia (FH) panel from their range of fully tested and optimised content.
The SureSeq myPanel NGS custom FH panel offers:
Hybridisation-based enrichment delivering unparalleled coverage, completeness and uniformity — detect variants with confidence and minimise the requirement for supplementary fill-in with Sanger sequencing
Detection of copy number variation (CNV) as well a single nucleotide variants (SNV) with a single assay
Pre-optimised panels that meet your technical requirements — no more laborious in-house optimisation, decreasing assay development time
Bespoke panel content — sequence only what’s relevant for your research, increase throughput and save on sequencing reagents
Custom CytoSure microarrays — available for confirmation of CNV detection
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Features of SureSeq myPanel™ NGS custom FH panel
Simply mix and match the gene and hotspot baits that you require for your research to enable analysis of both SNV and CNV from a single assay.
[u]Select from:[/u]
All exons:
LDLR
PCSK9
APOB
LDLRAP1
APOE
LIPA
STAP1
Hotspots:
rs2306283 (SLCO1B1)
rs4149056 (SLCO1B1)
rs11220462 Intronic region of ST3GAL4)
rs1564348 (Intronic region of SLC22A1)
rs1800562 (coding region on HFE)
rs2479409 (upstream of PCSK9)
rs3757354 (~2kb upstream of MYLIP)
rs4299376 (Intronic region of ABCG8)
rs629301 (3prime UTR of CELSR2)
rs6511720 (Intronic region on LDLR)
rs8017377 (coding region of NYNRIN)
rs1367117 (coding region of APOB)
rs429358 (coding region of APOE)
rs7412 (coding region of APOE)
General Specifications
There are no General Specifications available.