Associated Papers
Exome sequencing in patients with chronic central serous chorioretinopathy.
Schellevis RL et al.
Scientific Reports, 2019
31036833 (PubMed )
Supplement: 41598_2019_43152_MOESM1_ESM.pdf
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-AO-A03R-01A.domain
Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia.
Flanagan JM et al.
Blood, 2013
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