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The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research
Copy number variations (CNVs) are major causative contributors both in the genesis of genetic diseases and human neoplasias. While “High-Throughput” sequencing technologies are increasingly becoming the primary choice for genomic screening analysis, their ability to efficiently detect CNVs is still...
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| Izdano u: | F1000Res |
|---|---|
| Glavni autori: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
F1000 Research Limited
2020
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8311797/ https://ncbi.nlm.nih.gov/pubmed/34367618 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/f1000research.24887.1 |
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