PennCNV: An integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data

Click on image to view larger version.

Table 3.

A comparison of the number and size of CNVs in 112 HapMap individuals detected by three different technical platforms

Click on table to view larger version.

Table 3.

The PennCNV algorithm is used on the HumanHap550 platform without the use of family information.

This Article

  1. Published in Advance October 5, 2007, doi: 10.1101/gr.6861907 Genome Res. 17: 1665-1674

Preprint Server



Current Issue

  1. March 2026, 36 (3)
  1. Current Issue
  1. Alert me to new issues of Genome Research