An initial map of insertion and deletion (INDEL) variation in the human genome.

doi:10.1101/gr.4565806

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Article

An initial map of insertion and deletion (INDEL) variation in the human genome.

Genome research - 1 Sept 2006

Mills Ryan E, Luttig Christopher T, Larkins Christine E, Beauchamp Adam, Tsui Circe, Pittard W Stephen, Devine Scott E

Abstract excerpt

Although many studies have been conducted to identify single nucleotide polymorphisms (SNPs) in humans, few studies have been conducted to identify alternative forms of natural genetic variation, such as insertion and deletion (INDEL) polymorphisms. In this report, we describe an initial map of human INDEL variation that contains 415,436 unique INDEL polymorphisms. These INDELs were identified with a...

Topics

Animals
Computational Biology
Genome, Human
Humans
Pan troglodytes
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Sequence Deletion

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Identifiers

PMID: 16902084
DOI: 10.1101/gr.4565806
PMCID: PMC1557762

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