In this paper, the authors describe a technique to capture human exons on arrays then sequence them by Illumina 1G sequencing. It is hoped that this technique will identify new causes of diseases.
Nat Genet. 2007 Nov 4; [Epub ahead of print]
Hodges E, Xuan Z, Balija V, Kramer M, Molla MN, Smith SW, Middle CM, Rodesch MJ,
Albert TJ, Hannon GJ, McCombie WR.
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Philippe Campeau, MD
Resident in Medical Genetics at McGill University
OMMBID Blog Administrator