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Lecture-3 EXOME SEQUENCING Huseyin Tombuloglu, Phd GBE423 Genomics & Proteomics
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EXOME SEQUENCING
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͠ 1% of genome Mutations or variations in this portion of genome have severe consequences than in the remaining 99% Exome sequencing is especially effective in the study of rare Mendelian diseases EXOME SEQUENCING
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How it works?
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Target-enrichment strategies 1 PCR (Multiplex) 2 Molecular inversion probes (MIP) 3 Hybrid capture 4 In-solution capture 5 Sequencing
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Target-enrichment strategies 1 PCR (Multiplex) 2 Molecular inversion probes (MIP) 3 Hybrid capture 4 In-solution capture 5 Sequencing
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3 Hybrid capture Roche NimbleGen ~180,000 coding exons Agilent Capture Array Biotiniylated gene spesific probes Array technology
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4 In Solution Capture Probes in solution can capture all exons (exome) for high throughput sequencing Biotin-streptovidin based 1-2% of whole genome seq Easily multiplex 20 samples in one lane 11
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Comparative Sequencing WGS & WES
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The Case Somatic mutation detection between normal / cancer pairs WGS & WES ? 14 Meyerson et al, Nat Rev Genet 2010
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Figure 1 Steps in the generation of whole-genome or whole-exome sequencing data for analysis Foo, J.-N. et al. (2012) Whole-genome and whole-exome sequencing in neurological diseases Nat. Rev. Neurol. doi:10.1038/nrneurol.2012.148
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Clinical practices of Exome Sequencing
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Rare diseases Some rare diseases affect as many as 200,000 people, but some are so rare that they affect one or two people in the world.
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This was the first reported study that used exome sequencing as an approach to identify an unknown causal gene for a rare mendelian disorder (2009)
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Strategy to mine the Causal Gene
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Exome Sequencing Services The pilot program announced by 23andMe costs $999 and requires no physician signature, but provides only raw data without analysis. In November 2012, DNADTC, a division of Gene by Gene started offering exomes at 80X coverage and introductory price of $695. This price per DNADTC web site is currently $895. In October 2013, Beijing Genomics Institute (BGI) announced a promotion for personal whole exome sequencing at 50X coverage for $499
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1% of genome, limited size Usefull for large genomes, such as wheat, barley …etc Less complicated results, Cost effective Advantages
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Applications in other organisms
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