Custom Ophthalmic Research Panels

CD-Genomics offers a series of panel of ophthalmic diseases, including achromatopsia, cataract, glaucoma, Bardet-Biedl syndrome, Leber congenital amaurosis, retinitis pigmentosa, ectopia lentis, vitreoretinopathy, macular degeneration, and high myopia. Over 380 genes for you to choose from. Targeted NGS sequencing and Illumina MiSeq/Ion PGM system ensures high throughput and high-quality coverage to detect gene variation, so that we can obtain reliable results quickly, accurately and at low cost.

This panel contains 12 genes for your selection, such as ATF6, CNGA3, CNGB3, GNAT2, PDE6C, and PDE6H.

This panel contains 85 genes for your selection, including NHS, OCRL1, EBP, BCOR, COL4A5 and others.

This panel contains 50 genes for your selection, such as CYP1B1, MYOC, PXDN and other associated genes.

This panel contains 34 genes for your selection, such as BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP1/BBS18.

This panel contains 23 genes, including common pathogenic genes AIPL1, CEP290, CRB1, GUCY2D, RPE65 and new pathogenic gene NMNAT1, etc.

This panel contains 66 genes for your selection, such as MERTK, ERTK, and PRPF31.

This panel contains 25 genes for you to select, including ADAMTSL4, LTBP2, and FBN1, etc.

This panel contains 23 genes for you to select, including BEST1, CAPN5 and ZNF408, etc.

This panel contains 38 genes associated with macular degeneration, including ABCA4, CFH, CDH3, DRAM2, IMPG1, and CERKL, etc.

This panel contains 25 genes associated with high myopia, including LRPAP1, SLC39A5, SCO2 and PRIMPOL, etc.

* For Research Use Only. Not for use in diagnostic procedures.

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