Biostatistics 666: Analysis of Copy Number Using Sequence Data

From Genome Analysis Wiki
Jump to navigationJump to search
The printable version is no longer supported and may have rendering errors. Please update your browser bookmarks and please use the default browser print function instead.

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

Slides in PDF Format

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