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Small insertions and deletions (INDELs) in human genomes

2010; Oxford University Press; Volume: 19; Issue: R2 Linguagem: Inglês

10.1093/hmg/ddq400

1460-2083

Julienne M. Mullaney, Ryan E. Mills, W. Stephen Pittard, Scott E. Devine,

Genomics and Chromatin Dynamics

In this review, we focus on progress that has been made with detecting small insertions and deletions (INDELs) in human genomes. Over the past decade, several million small INDELs have been discovered in human populations and personal genomes. The amount of genetic variation that is caused by these small INDELs is substantial. The number of INDELs in human genomes is second only to the number of single nucleotide polymorphisms (SNPs), and, in terms of base pairs of variation, INDELs cause similar levels of variation as SNPs. Many of these INDELs map to functionally important sites within human genes, and thus, are likely to influence human traits and diseases. Therefore, small INDEL variation will play a prominent role in personalized medicine.