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书目名称Cell-free DNA as Diagnostic Markers影响因子(影响力)<br> http://impactfactor.cn/2024/if/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers影响因子(影响力)学科排名<br> http://impactfactor.cn/2024/ifr/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers网络公开度<br> http://impactfactor.cn/2024/at/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers网络公开度学科排名<br> http://impactfactor.cn/2024/atr/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers被引频次<br> http://impactfactor.cn/2024/tc/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers被引频次学科排名<br> http://impactfactor.cn/2024/tcr/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers年度引用<br> http://impactfactor.cn/2024/ii/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers年度引用学科排名<br> http://impactfactor.cn/2024/iir/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers读者反馈<br> http://impactfactor.cn/2024/5y/?ISSN=BK0222955<br><br> <br><br>书目名称Cell-free DNA as Diagnostic Markers读者反馈学科排名<br> http://impactfactor.cn/2024/5yr/?ISSN=BK0222955<br><br> <br><br>围巾 发表于 2025-3-21 22:23:24
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Cell-Free DNA Integrity: Applicationsen studied for cfDNAi, such as specific genes involved in cancer progression or repetitive DNA sequences as surrogate markers for the whole circulating DNA..However, the lack of a standardized method for cfDNAi evaluation remains one of its main critical issues. Apoptotic index (AI) and integrity inpanorama 发表于 2025-3-22 13:26:41
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Studying Copy Number Variations in Cell-Free DNA: The Example of AR in Prostate Cancerrting from the hypothesis that the gain of androgen receptor (.) gene is a frequent aberration in advanced prostate cancer patients, we analyzed it in cfDNA as a potential predictive biomarker of specific treatments. Here we report a general protocol that may be considered to analyze gene copy numbe胰脏 发表于 2025-3-22 22:37:13
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From cfDNA to Sequencing: Workflows and Potentialsesistance by following the mutation status changes of patients. In this field, high-sensitivity methods like next-generation sequencing (NGS) could help to accurately detect somatic mutations at low frequency. Here, we report some advantages and limitations of NGS approaches for cfDNA mutation analyLUDE 发表于 2025-3-23 06:24:13
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