Quadruplex MAPH: improvement of throughput in high-resolution copy number screening
<p>Abstract</p> <p>Background</p> <p>Copy number variation (CNV) in the human genome is recognised as a widespread and important source of human genetic variation. Now the challenge is to screen for these CNVs at high resolution in a reliable, accurate and cost-effectiv...
| Published in: | BMC Genomics |
|---|---|
| Main Authors: | , , , |
| Format: | Article |
| Language: | English |
| Published: |
BMC
2009-09-01
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| Online Access: | http://www.biomedcentral.com/1471-2164/10/453 |
