Difference between revisions of "Biostatistics 666: Analysis of Copy Number Using Sequence Data"
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| − | * Handsaker, Korn, Nemesh and McCarroll (2011) | + | * Handsaker, Korn, Nemesh and McCarroll (2011) Discovery and genotyping of genome structural polymorphism by sequencing on a population scale. ''Nature Genetics'' '''43''':269 - 276 |
Latest revision as of 09:14, 5 December 2011
Overview
Introduces the analysis of copy number variation using next generation sequence data, discussing the types of evidence that can be observed in one individual and also in a population of individuals where a copy number variant is segregating.
Slides
Recommended Reading
- Handsaker, Korn, Nemesh and McCarroll (2011) Discovery and genotyping of genome structural polymorphism by sequencing on a population scale. Nature Genetics 43:269 - 276
