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Exome Sequencing
TACGen offers a high throughput exome sequencing service to support variant discovery.
Sample Submission:
Accepted starting materials:
- Genomic DNA derived from cell lines, fresh frozen tissue,
- Premade Capture Libraries ready for Illumina sequencing
Work Flow:
- Illumina paired-end library construction
- Target-enrichment
- Sequencing on Illumina platform
Applications:
- Rare variant mapping in complex disorders
- Discovery of Mendelian disorders
- Clinical diagnostics
Additional Services:
- Whole genome amplification
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