A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation
<p>Abstract</p> <p>Copy number variants (CNVs) create a major source of variation among individuals and populations. Array-based comparative genomic hybridisation (aCGH) is a powerful method used to detect and compare the copy numbers of DNA sequences at high resolution along the g...
| প্রধান লেখক: | , , , , |
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| বিন্যাস: | প্রবন্ধ |
| ভাষা: | English |
| প্রকাশিত: |
BMC
2010-08-01
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| মালা: | Human Genomics |
| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | http://www.humgenomics.com/content/4/6/421 |