• 1-631-338-8059        
x

Custom Ophthalmic Research Panels

Inquiry

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.

Services
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 purposes only, not intended for clinical diagnosis, treatment, or individual health assessments.
Related Sections

Related Services:

Solid Tumor Panel Sequencing (500 genes)
Custom Vitreoretinopathy Panel
Custom Celiac Disease Panel
Custom Familial Hypercholesterolemia Panel
Custom Hearing Loss Research Panel
Custom Renal Cancer Panel
Custom Comprehensive Cardiomyopathy Panel
Breast Cancer Panel Sequencing
Bioinformatics Analysis Service

Related Resource:

Faster and More Precise NGS for Disease Panel: Hybridization Capture-Based Target Enrichment
Overview of Gene Target Enrichment Methods for Disease Research
MassArray for Virus Detection: Introduction, Features, and Applications
How Does Amplicon Based Target Enrichment Work for Disease Panel
Multiplex Ligation-dependent Probe Amplification (MLPA): Specifications, Pros & Cons, and Applications in Disease Research
Workflow and Methodology for TMB Assessment in Solid Tumors
NGS-Based Disease Panel of Great Importance in Research, for the Better Healthcare and Treatment
Targeted Sequencing Panel: Applications and Analysis of Targeted Genomic Sequencing in Disease Studies
What Are Cancer Panels and What Can They Detect?
PDF Download
* Email Address:

CD Genomics needs the contact information you provide to us in order to contact you about our products and services and other content that may be of interest to you. By clicking below, you consent to the storage and processing of the personal information submitted above by CD Genomcis to provide the content you have requested.

×
  • SUITE 111, 17 Ramsey Road, Shirley, NY 11967, USA
  • 1-631-338-8059
  • 1-631-614-7828
Copyright © 2025 CD Genomics. All rights reserved.
Top
0
Inquiry Basket
There is no product in the inquiry basket.

We use cookies to understand how you use our site and to improve the overall user experience. This includes personalizing content and advertising. Read our Privacy Policy

Accept Cookies
x