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. 2010 Mar 1;24(5):423–431. doi: 10.1101/gad.1864110

Figure 4.

Figure 4.

Methods for detecting variation in a human genome sequence using DNA sequencing technologies. (A) Paired-end reads to detect insertions and deletions. (B) Split read methods for breakpoint idnetification. (C) Read depth analysis to detect CNVs. (D) Local reassembly to reconstruction novel insertions.

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