Related Articles
Characterization of pancreatic ductal adenocarcinoma using whole transcriptome sequencing and copy number analysis by single-nucleotide polymorphism array
Visual inspection reveals a novel pathogenic mutation in <em>PKD1</em> missed by the variant caller in whole‑exome sequencing
Somatic mutations in myeloid cell leukemia‑1 contribute to the pathogenesis of glioma by prolonging its half‑life
Identification of a novel mutation in CRYM in a Chinese family with hearing loss using whole‑exome sequencing
Clinical application of whole-exome sequencing: A retrospective, single-center study