טוען...
Increasing the diagnostic yield of exome sequencing by copy number variant analysis
As whole exome sequencing (WES) becomes more widely used in the clinical realm, a wealth of unanalyzed information will be routinely generated. Using WES read depth data to predict copy number variation (CNV) could extend the diagnostic utility of this previously underutilized data by providing clin...
שמור ב:
| הוצא לאור ב: | PLoS One |
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| Main Authors: | , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Public Library of Science
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6296659/ https://ncbi.nlm.nih.gov/pubmed/30557390 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0209185 |
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