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Article

Polymorphisms and rare variants identified by next-generation sequencing confer risk for lung cancer in han Chinese population.

Pathology, research and practice - 1 Apr 2020

Li Xiaoqi, Liu Jinsheng, Wang Ke, Zhou Juan, Zhang Hang, Zhang Mancang, Shi Yongyong

Abstract excerpt

BACKGROUND: Lung cancer is one of the leading causes of cancer death worldwide, and genetic risk factors account for a large part of its carcinogenesis. The low economic requirements and high efficiency of next-generation sequencing (NGS) make it widely used in detecting genetic alterations in pathogenesis. METHODS: We performed targeted panel sequencing in 780 Han Chinese lung cancer patients using a commercial...

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PMID: 32107087
DOI: 10.1016/j.prp.2020.152873

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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