Accurate and reliable high-throughput detection of copy number variation in the human genome

This study describes a new tool for accurate and reliable high-throughput detection of copy number variation in the human genome. We have constructed a large-insert clone DNA microarray covering the entire human genome in tiling path resolution that we have used to identify copy number variation in...

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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Fiegler, Heike, Redon, Richard, Andrews, Dan, Scott, Carol, Andrews, Robert, Carder, Carol, Clark, Richard, Dovey, Oliver, Ellis, Peter, Feuk, Lars, French, Lisa, Hunt, Paul, Kalaitzopoulos, Dimitrios, Larkin, James, Montgomery, Lyndal, Perry, George H., Plumb, Bob W., Porter, Keith, Rigby, Rachel E., Rigler, Diane, Valsesia, Armand, Langford, Cordelia, Humphray, Sean J., Scherer, Stephen W., Lee, Charles, Hurles, Matthew E., Carter, Nigel P.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Cold Spring Harbor Laboratory Press 2006
Θέματα:
Methods
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1665640/
https://ncbi.nlm.nih.gov/pubmed/17122085
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/gr.5630906
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