Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays.

Optimizing copy number variation analysis using genome-wide short sequence oligonucleotide arrays. Nucleic Acids Res. 2010 Jun; 38(10):3275-86.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.