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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 (515 reads)

Structural Insights into RbmA, a Biofilm Scaffolding Protein of V. Cholerae. (2013) PLoS ONE (481 reads)

DriverDB: an exome sequencing database for cancer driver gene identification. (2014) Nucleic Acids Research (536 reads)

Proposed Carrier Lipid-Binding Site of Undecaprenyl Pyrophosphate Phosphatase from Escherichia coli. (2014) The Journal of Biological Chemistry (504 reads)

SeqSIMLA2: Simulating Correlated Quantitative Traits Accounting for Shared Environmental Effects in User-Specified Pedigree Structure. (2014) Genetic Epidemiology (709 reads)

Family-Based Association Test Using Both Common and Rare Variants and Accounting for Directions of Effects for Sequencing Data. (2014) PLoS ONE (661 reads)

YM500v2: a small RNA sequencing (smRNA-seq) database for human cancer miRNome research. (2014) Nucleic Acids Research (760 reads)

Crowning Proteins: Modulating the Protein Surface Properties using Crown Ethers. (2014) Angewandte Chemie International Edition (687 reads)

Reciprocal allosteric regulation of p38g and PTPN3 involves a PDZ domain–modulated complex formation. (2014) Science Signaling (658 reads)

Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing. (2014) Mutation Research (811 reads)

Hierarchical Clustering of Breast Cancer Methylomes Revealed Differentially Methylated and Expressed Breast Cancer Genes. (2015) PLOS One (777 reads)

Substrate Specificity and Plasticity of FERM-Containing Protein Tyrosine Phosphatases. (2015) Structure (1613 reads)

A multi-SNP association test for complex diseases incorporating an optimal P-value threshold algorithm in nuclear families. (2015) PLOS One (1637 reads)

DNA Demethylation Dynamics in the Human Prenatal Germline. (2015) Cell (1656 reads)

Complete Taiwanese Macaque (Macaca cyclopis) Mitochondrial Genome: Reference-Assisted de novo Assembly with Multiple kmer Strategy. (2015) PLOS One (1422 reads)

Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. (2015) Nat Commun (1474 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 (1502 reads)

Identifying Children With Poor Cochlear Implantation Outcomes Using Massively Parallel Sequencing. (2015) Medicine(Baltimore) (1489 reads)

Structural D/E-rich repeats play multiple roles especially in gene regulation through DNA/RNA mimicry. (2015) Molecular BioSystems (1400 reads)

Two Novel De Novo GARS Mutations Cause Early-Onset Axonal Charcot-Marie-Tooth Disease. (2015) PLOS One (1417 reads)

DriverDBv2: a database for human cancer driver gene research. (2015) Nucleic Acids Research (1429 reads)

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