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Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.
Chang TY, Chung IF, Wu WJ, Chang SP, Lin WH, Ginsberg NA, Ma GC, Chen M. Chang TY, et al. Among authors: chang sp. Diagnostics (Basel). 2020 May 7;10(5):286. doi: 10.3390/diagnostics10050286. Diagnostics (Basel). 2020. PMID: 32392875 Free PMC article.
DriverDB: an exome sequencing database for cancer driver gene identification.
Cheng WC, Chung IF, Chen CY, Sun HJ, Fen JJ, Tang WC, Chang TY, Wong TT, Wang HW. Cheng WC, et al. Among authors: chang ty. Nucleic Acids Res. 2014 Jan;42(Database issue):D1048-54. doi: 10.1093/nar/gkt1025. Epub 2013 Nov 7. Nucleic Acids Res. 2014. PMID: 24214964 Free PMC article.
Comprehensive evaluation of fusion transcript detection algorithms and a meta-caller to combine top performing methods in paired-end RNA-seq data.
Liu S, Tsai WH, Ding Y, Chen R, Fang Z, Huo Z, Kim S, Ma T, Chang TY, Priedigkeit NM, Lee AV, Luo J, Wang HW, Chung IF, Tseng GC. Liu S, et al. Among authors: chang ty. Nucleic Acids Res. 2016 Mar 18;44(5):e47. doi: 10.1093/nar/gkv1234. Epub 2015 Nov 17. Nucleic Acids Res. 2016. PMID: 26582927 Free PMC article.
A Silicon-based Coral-like Nanostructured Microfluidics to Isolate Rare Cells in Human Circulation: Validation by SK-BR-3 Cancer Cell Line and Its Utility in Circulating Fetal Nucleated Red Blood Cells.
Ma GC, Lin WH, Huang CE, Chang TY, Liu JY, Yang YJ, Lee MH, Wu WJ, Chang YS, Chen M. Ma GC, et al. Among authors: chang ys, chang ty. Micromachines (Basel). 2019 Feb 17;10(2):132. doi: 10.3390/mi10020132. Micromachines (Basel). 2019. PMID: 30781548 Free PMC article.
1,071 results