Genomika, Bio-medicína a Sekvenování DNA : Přítomnost a Perspektivy
Místo konání: CTS, Husova 4, Praha 1, 3. patro
Přednáší: Wilhelm Ansorge
Přehled vývoje techniky, její aplikace v biomedicíně, perspektivní přínos pro analýzu a terapii nemoci. Více se lze dočíst např. v článku W. Ansorge, Next Generation DNA Sequencing Techniques, New Biotechnology, vol. 25, 4/2009, str. 195-203, jehož abstrakt uvádíme níže a jehož celý text na požádání zašleme. Next-generation high-throughput DNA sequencing techniques are opening fascinating opportunities in the life sciences. Novel fields and applications in biology and medicine are becoming a reality, beyond the genomic sequencing which was original development goal and application. Serving as examples are: personal genomics with detailed analysis of individual genome stretches; precise analysis of RNA transcripts for gene expression, surpassing and replacing in several respects analysis by various microarray platforms, for instance in reliable and precise quantification of transcripts and as a tool for identification and analysis of DNA regions interacting with regulatory proteins in functional regulation of gene expression. The next-generation sequencing technologies offer novel and rapid ways for genome-wide characterisation and profiling of mRNAs, small RNAs, transcription factor regions, structure of chromatin and DNA methylation patterns, microbiology and metagenomics. In this article, development of commercial sequencing devices is reviewed and some European contributions to the field are mentioned. Presently commercially available very high-throughput DNA sequencing platforms, as well as techniques under development, are described and their applications in bio-medical fields discussed.