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CoNVaQ: a web tool for copy number variation-based association studies
BACKGROUND: Copy number variations (CNVs) are large segments of the genome that are duplicated or deleted. Structural variations in the genome have been linked to many complex diseases. Similar to how genome-wide association studies (GWAS) have helped discover single-nucleotide polymorphisms linked...
Shranjeno v:
| izdano v: | BMC Genomics |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2018
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5960125/ https://ncbi.nlm.nih.gov/pubmed/29776329 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12864-018-4732-8 |
| Oznake: |
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