CDCap™ Human Hemoglobin Gene Panel for enrichment of human hemoglobin coding genes, adjacent genomic regions, and regulatory genes. The Panel targets a 160 Kb genomic region to comprehensively enrich sequence information on multiple variants associated with human hemoglobin.
For Hemoglobin Coding Genes
· Covers regions within 1 Kb upstream and downstream of hemoglobin coding genes, enriching various sequence variants in coding and non-coding regions.
For Gene Cluster Regions
· Covers high-density SNP backbone regions and utilizes highly heterozygous SNP loci to improve analytical power for copy number variation across the entire region.
For Known Structural Mutations
· Covers breakpoint locations of known structural mutations, enabling direct analysis of structural rearrangements through split-read analysis.
For Regulatory Genes and Variants
· Covers coding regions of regulatory genes (BCL11A, HBS1L, KLF1, MYB) and 30 polymorphic sites in non-coding regions.
| Enrichment Method: | Probe Hybridization Capture |
| Species: | Human |
| Variant Types: | SNV、SV、Complex Rearrangements |
| Target Size: | 160Kb |
| Sample Type: | blood、swab etc. |
| Method: | NGS |
| Sequencing Platform: | Illumina |
| Storage: | Store at -20 °C. |
1. Capture Performance
2. Multiple Variants Analysis
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