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This is Section 論文致謝.
Following are the articles published under this section.

Identification of latent biomarkers in hepatocellular carcinoma by ultra-deep whole-transcriptome sequencing. (2013) Oncogene (468 reads)

Structural Insights into RbmA, a Biofilm Scaffolding Protein of V. Cholerae. (2013) PLoS ONE (435 reads)

DriverDB: an exome sequencing database for cancer driver gene identification. (2014) Nucleic Acids Research (493 reads)

Proposed Carrier Lipid-Binding Site of Undecaprenyl Pyrophosphate Phosphatase from Escherichia coli. (2014) The Journal of Biological Chemistry (452 reads)

SeqSIMLA2: Simulating Correlated Quantitative Traits Accounting for Shared Environmental Effects in User-Specified Pedigree Structure. (2014) Genetic Epidemiology (660 reads)

Family-Based Association Test Using Both Common and Rare Variants and Accounting for Directions of Effects for Sequencing Data. (2014) PLoS ONE (617 reads)

YM500v2: a small RNA sequencing (smRNA-seq) database for human cancer miRNome research. (2014) Nucleic Acids Research (690 reads)

Crowning Proteins: Modulating the Protein Surface Properties using Crown Ethers. (2014) Angewandte Chemie International Edition (635 reads)

Reciprocal allosteric regulation of p38g and PTPN3 involves a PDZ domain–modulated complex formation. (2014) Science Signaling (607 reads)

Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing. (2014) Mutation Research (736 reads)

Hierarchical Clustering of Breast Cancer Methylomes Revealed Differentially Methylated and Expressed Breast Cancer Genes. (2015) PLOS One (729 reads)

Substrate Specificity and Plasticity of FERM-Containing Protein Tyrosine Phosphatases. (2015) Structure (1543 reads)

A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. (2015) PLOS One (1553 reads)

DNA Demethylation Dynamics in the Human Prenatal Germline. (2015) Cell (1586 reads)

Complete Taiwanese Macaque (Macaca cyclopis) Mitochondrial Genome: Reference-Assisted de novo Assembly with Multiple kmer Strategy. (2015) PLOS One (1342 reads)

Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. (2015) Nat Commun (1393 reads)

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 (1429 reads)

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing. (2015) Medicine(Baltimore) (1396 reads)

Structural D/E-rich repeats play multiple roles especially in gene regulation through DNA/RNA mimicry. (2015) Molecular BioSystems (1328 reads)

Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease. (2015) PLOS One (1338 reads)

DriverDBv2: a database for human cancer driver gene research. (2015) Nucleic Acids Research (1346 reads)

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