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Detection of cell‐free DNA fragmentation and copy number alterations in cerebrospinal fluid from glioma patients
Glioma is difficult to detect or characterize using current liquid biopsy approaches. Detection of cell‐free tumor DNA (cftDNA) in cerebrospinal fluid (CSF) has been proposed as an alternative to detection in plasma. We used shallow whole‐genome sequencing (sWGS, at a coverage of < 0.4×) of cell‐...
שמור ב:
| הוצא לאור ב: | EMBO Mol Med |
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| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
John Wiley and Sons Inc.
2018
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6284385/ https://ncbi.nlm.nih.gov/pubmed/30401727 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.201809323 |
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