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這是專欄 論文致謝.
專欄文章一覽

Identification of latent biomarkers in hepatocellular carcinoma by ultra-deep whole-transcriptome sequencing. (2013) Oncogene (358 閱讀)

Structural Insights into RbmA, a Biofilm Scaffolding Protein of V. Cholerae. (2013) PLoS ONE (321 閱讀)

DriverDB: an exome sequencing database for cancer driver gene identification. (2014) Nucleic Acids Research (380 閱讀)

Proposed Carrier Lipid-Binding Site of Undecaprenyl Pyrophosphate Phosphatase from Escherichia coli. (2014) The Journal of Biological Chemistry (328 閱讀)

SeqSIMLA2: Simulating Correlated Quantitative Traits Accounting for Shared Environmental Effects in User-Specified Pedigree Structure. (2014) Genetic Epidemiology (551 閱讀)

Family-Based Association Test Using Both Common and Rare Variants and Accounting for Directions of Effects for Sequencing Data. (2014) PLoS ONE (499 閱讀)

YM500v2: a small RNA sequencing (smRNA-seq) database for human cancer miRNome research. (2014) Nucleic Acids Research (543 閱讀)

Crowning Proteins: Modulating the Protein Surface Properties using Crown Ethers. (2014) Angewandte Chemie International Edition (517 閱讀)

Reciprocal allosteric regulation of p38g and PTPN3 involves a PDZ domain–modulated complex formation. (2014) Science Signaling (489 閱讀)

Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing. (2014) Mutation Research (573 閱讀)

Hierarchical Clustering of Breast Cancer Methylomes Revealed Differentially Methylated and Expressed Breast Cancer Genes. (2015) PLOS One (587 閱讀)

Substrate Specificity and Plasticity of FERM-Containing Protein Tyrosine Phosphatases. (2015) Structure (1331 閱讀)

A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. (2015) PLOS One (1336 閱讀)

DNA Demethylation Dynamics in the Human Prenatal Germline. (2015) Cell (1337 閱讀)

Complete Taiwanese Macaque (Macaca cyclopis) Mitochondrial Genome: Reference-Assisted de novo Assembly with Multiple kmer Strategy. (2015) PLOS One (1011 閱讀)

Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. (2015) Nat Commun (1096 閱讀)

Concurrent exome-targeted next-generation sequencing and single nucleotide polymorphism array to identify the causative genetic aberrations of isolated Mayer-Rokitansky-Küster-Hauser syndrome. (2015) Hum Reprod (1155 閱讀)

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing. (2015) Medicine(Baltimore) (1108 閱讀)

Structural D/E-rich repeats play multiple roles especially in gene regulation through DNA/RNA mimicry. (2015) Molecular BioSystems (1099 閱讀)

Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease. (2015) PLOS One (1130 閱讀)

DriverDBv2: a database for human cancer driver gene research. (2015) Nucleic Acids Research (1082 閱讀)

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