High-resolution identification of chromosomal abnormalities using oligonucleotide arrays containing 116,204 SNPs
uncertainWhole-genome genotyping platforms
- Journal
- American Journal of Human Genetics
- Published
- 2005
- Record
- ↗ Journal record
Synopsis
A high-throughput approach for assessing DNA copy-number changes with high-density oligonucleotide arrays containing 116,204 SNPs, detecting amplifications and deletions over a wide range of sizes. The finder reported Kennedy as a senior author, but no retrieved record shows the author list, so her authorship is recorded as an open question.