<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(2)</volume><submitter>Cui S</submitter><pubmed_abstract>Capture-based next-generation sequencing (NGS) is a potentially useful diagnostic method to measure tumor tissue DNA in blood as it can identify concordant mutations between cell-free DNA (cfDNA) and primary tumor DNA in lung cancer patients. In this study, the sensitivity, specificity and accuracy of capture-based NGS for detecting ALK fusion in plasma cfDNA was assessed. 24 patients with tissue ALK-positivity and 15 who did not harbor ALK fusion were enrolled. 13 ALK-positive samples were identified by capture-based NGS among the 24 samples with tissue ALK-positivity. In addition to EML4-ALK, 2 rare fusion types (FAM179A-ALK and COL25A1-ALK) were also identified. The overall sensitivity, specificity and accuracy for all cases were 54.2%, 100% and 71.8%, respectively. For patients without</pubmed_abstract><journal>Oncotarget</journal><pagination>2771-2780</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5356840</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Use of capture-based next-generation sequencing to detect ALK fusion in plasma cell-free DNA of patients with non-small-cell lung cancer.</pubmed_title><pmcid>PMC5356840</pmcid><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Xiong L</pubmed_authors><pubmed_authors>Jiang L</pubmed_authors><pubmed_authors>Chu T</pubmed_authors><pubmed_authors>Pan F</pubmed_authors><pubmed_authors>Wang H</pubmed_authors><pubmed_authors>Cui S</pubmed_authors><pubmed_authors>Zhao Y</pubmed_authors><pubmed_authors>Niu Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Use of capture-based next-generation sequencing to detect ALK fusion in plasma cell-free DNA of patients with non-small-cell lung cancer.</name><description>Capture-based next-generation sequencing (NGS) is a potentially useful diagnostic method to measure tumor tissue DNA in blood as it can identify concordant mutations between cell-free DNA (cfDNA) and primary tumor DNA in lung cancer patients. In this study, the sensitivity, specificity and accuracy of capture-based NGS for detecting ALK fusion in plasma cfDNA was assessed. 24 patients with tissue ALK-positivity and 15 who did not harbor ALK fusion were enrolled. 13 ALK-positive samples were identified by capture-based NGS among the 24 samples with tissue ALK-positivity. In addition to EML4-ALK, 2 rare fusion types (FAM179A-ALK and COL25A1-ALK) were also identified. The overall sensitivity, specificity and accuracy for all cases were 54.2%, 100% and 71.8%, respectively. For patients without</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Jan</publication><modification>2025-04-04T14:33:24.564Z</modification><creation>2019-03-26T23:46:30Z</creation></dates><accession>S-EPMC5356840</accession><cross_references><pubmed>27926526</pubmed><doi>10.18632/oncotarget.13741</doi></cross_references></HashMap>