Associated Papers
Whole-exome sequencing in a Japanese multiplex family identifies new susceptibility genes for intracranial aneurysms.
Maegawa T et al.
Plos One, 2022
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A8-A06Y-01A.domain
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