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GATC Biotech introduces cross-platform barcoding system for
Unlike other methods, GATC’s system is suitable for use with the Roche GS FLX and Illumina Genome Analyzer. This barcoding method is especially well suited to DNA smaller than whole genomes (e.g. cDNA libraries, de novo sequencing of BACs, fosmids, viruses) whose sequencing would otherwise be impractical and expensive. The technique is highly efficient, resulting in 99.9% of sequences successfully tagged, which lead to dramatic cost savings.
Thomas Pohl, CTO of GATC Biotech, said: “We saw the need for a platform-independent barcoding system that was not limited by the number of tags used. We optimised the length of the tags so that they are sufficient for high-quality sequence sorting but also make the data loss acceptable when using Next-Gen sequencers which produce micro reads of 36 bases or less. Moreover, these sequencers are now a cost-effective option for de novo sequencing of, for example, organelles such as chloroplasts or mtDNA, as the number of micro reads is relatively low. We use DNASTAR’s SeqMan Genome Assembler for the assembly.”
The barcoding system is now available to GATC Biotech’s next-generation sequencing customers. The system has already been successfully applied to BAC sequencing projects with 50 individual tags using the GS FLX. Additionally, in cooperation with Prof. Dr. Christof von Kalle and Dr. Manfred Schmidt of the NCT in Heidelberg, GATC Biotech has used barcoding to improve the sequencing efficiency within the ongoing EU funded CONSERT project. The research project was set up to develop and improve gene therapy protocols for inherited diseases.
Contact: GATC Biotech AG Senior Director Marketing |
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