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- Develop a toolbox of methods for the selective enrichment of specific regions of the genome under simultaneous
reduction of the complexity of the sample.
- Define a standard format for data output from 2nd generation sequencing technologies and platforms.
- Contributions towards norms for display and integration of short sequence reads (SSRs) into public databases.
- Identify and implement data reduction schemes for three major application areas – Deep-resequencing ("medical resequencing"), copy number variation, and gene expression analysis.
- Define standards for quality scores of 2 nd generation nucleic acid sequencers.
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