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Article

The Clinical Relevance of Frequent Germline Genetic Variants Detected by Targeted Sequencing in Patients With Rectal Adenocarcinoma (READ).

Cancer genomics & proteomics - 1 Jan 2000

Huang Kevin Chih-Yang, Chiang Shu-Fen, Ke Tao-Wei, Chen William Tzu-Liang, Chen Tsung-Wei, Chao Kun-San Clifford

Abstract excerpt

BACKGROUND: The progression of colorectal cancer (CRC) mainly stems from the occurrence of somatic mutation. However, there is little information that can be used to comprehensively analyse the importance of germline variants in CRC patients. PATIENTS AND METHODS: The candidate germline variants between tumor relapse and cured rectal adenocarcinoma (READ) were firstly filtered by whole-exome sequencing (n=4), and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 32345670
DOI: 10.21873/cgp.20189
PMCID: PMC7259889

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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