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Preprocessing Sequence Coverage Data for More Precise Detection of Copy Number Variations
Copy number variation (CNV) is a type of genomic/genetic variation that plays an important role in phenotypic diversity, evolution, and disease susceptibility. Next generation sequencing (NGS) technologies have created an opportunity for more accurate detection of CNVs with higher resolution. Howeve...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | IEEE/ACM Trans Comput Biol Bioinform |
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| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2018
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7278033/ https://ncbi.nlm.nih.gov/pubmed/30222580 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1109/TCBB.2018.2869738 |
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