• 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:

Custom Inherited Disease Panels
Custom Comprehensive Cardiomyopathy Panel
Amplicon Sequencing-Based NGS Panel
Pathogens Detection
Drug Safety for Children
Custom Thrombocytopenia Panel
Custom Cardiomyopathy and Skeletal Muscle Diseases Panel
Custom MDS/MPN Overlap Panel
Custom Ovarian Cancer Panel

Related Resource:

Multiplex SNaPshot Assay-Based SNP Analysis for Disease Panel
How Does Next-Generation Sequencing Guide Cancer Detection and Therapy
Applications
MassARRAY, A High-Precision and Cost-Effective Technology for Cancer Research
Deciphering the Role of Long Non-Coding RNA in Cancer Research
MassArray for Virus Detection: Introduction, Features, and Applications
Bioinformatics Facilitating NGS-Based Methods in Pathogen Detection
ARMS-PCR in Disease Research: Principle, Sequence Variation Analysis, and Application
Sequencing Methods for Tumor Profiling and Mutation Load in Cancer Research
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

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