Titlebook: Cell-free DNA as Diagnostic Markers; Methods and Protocol Valentina Casadio,Samanta Salvi Book 2019 Springer Science+Business Media, LLC, p

digestive-tract

書目名稱Cell-free DNA as Diagnostic Markers影響因子(影響力)




書目名稱Cell-free DNA as Diagnostic Markers影響因子(影響力)學(xué)科排名




書目名稱Cell-free DNA as Diagnostic Markers網(wǎng)絡(luò)公開度




書目名稱Cell-free DNA as Diagnostic Markers網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Cell-free DNA as Diagnostic Markers被引頻次




書目名稱Cell-free DNA as Diagnostic Markers被引頻次學(xué)科排名




書目名稱Cell-free DNA as Diagnostic Markers年度引用




書目名稱Cell-free DNA as Diagnostic Markers年度引用學(xué)科排名




書目名稱Cell-free DNA as Diagnostic Markers讀者反饋




書目名稱Cell-free DNA as Diagnostic Markers讀者反饋學(xué)科排名

圍巾

deciduous

驕傲

無彈性

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 in

panorama

panorama

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

胰臟

飛來飛去真休

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 analy

LUDE