Abstract
Tumors are often polyclonal and are therefore heterogenous in their genomic and molecular profiles, which contributes to drug resistance and treatment failure. The methods used to detect these heterogenous differences in tumor samples are critical, but findings have been hindered by methodological inability to detect low-frequency subclones in bulk DNA. Chang et al. (2020) have addressed some of these methodological issues.
| Originalsprache | English |
|---|---|
| Seiten (von - bis) | 1501-1503 |
| Seitenumfang | 3 |
| Fachzeitschrift | Journal of Investigative Dermatology |
| Jahrgang | 140 |
| Ausgabenummer | 8 |
| Frühes Online-Datum | 21 Juli 2020 |
| DOIs |
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| Publikationsstatus | Published - 1 Aug. 2020 |
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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Good health and well being
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