While NGS offers unprecedented options in terms of high throughput sequencing. Sanger sequencing remains the gold standard for validation of variants, fast genotyping of Single Nucleotide Variants and in case of small sample sizes with a limited size of the Target sequence.
The CFG owns several ABI 3730 instruments for conventional Sanger Sequencing and Fragment Analysis.
Samples can be registered and handed in through our lab automation system, through which the sequencing results can also be downloaded after sequencing. The sequencing itself will be performed by our lab specialists.
To start using the Sanger sequencing service please contact us.