Genome-wide detection of segmental duplications and potential assembly errors in the human genome sequence.

Cheung J, Estivill X, Khaja R, MacDonald JR, Lau K, Tsui LC, Scherer SW
Genome Biol. 2003 4 (4): R25

PMID: 12702206 · PMCID: PMC154576 · DOI:10.1186/gb-2003-4-4-r25

MeSH Terms (11)

Artifacts Base Sequence Chromosomes, Human Computational Biology Gene Duplication Genetic Diseases, Inborn Genetic Variation Genome, Human Humans Polymorphism, Single Nucleotide Sequence Analysis, DNA

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