Shilin Zhao

发表

Strategies for processing and quality control of Illumina genotyping arrays

Yan Guo, Shyr Yu, David C. Samuels, 2018, Briefings Bioinform..

Clinical Applications of Next Generation Sequencing

Shilin Zhao, 2014 .

NGSPERL: a semi-automated framework for large scale next generation sequencing data analysis

Quanhu Sheng, Shyr Yu, Mingsheng Guo, 2015, Int. J. Comput. Biol. Drug Des..

Heatmap3: an improved heatmap package with more powerful and convenient features

Yan Guo, Quanhu Sheng, Shyr Yu, 2014, BMC Bioinformatics.

RnaSeqSampleSize: real data based sample size estimation for RNA sequencing

Yan Guo, Quanhu Sheng, Shyr Yu, 2018, BMC Bioinformatics.

Detection of internal exon deletion with exon Del

Yan Guo, Quanhu Sheng, Thomas Stricker, 2014, BMC Bioinformatics.

Non-canonical RNA-DNA differences and other human genomic features are enriched within very short tandem repeats

Yan Guo, Quanhu Sheng, Hui Yu, 2020, PLoS Comput. Biol..

Gene and isoform expression signatures associated with tumor stage in kidney renal clear cell carcinoma

Qi Liu, Shyr Yu, Pei-Fang Su, 2013, BMC Systems Biology.

Tri-allelic heteroplasmies, DNA-RNA differences and their polynucleotide tract associations in the mitochondrial genome.

Yan Guo, David C. Samuels, Shilin Zhao, 2017, Genomics.

Transcriptome-wide signatures of tumor stage in kidney renal clear cell carcinoma: connecting copy number variation, methylation and transcription factor activity

Yu Shyr, Qi Liu, Pei-Fang Su, 2014, Genome Medicine.

Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants

Lisa Bastarache, Joshua C Denny, Dan M Roden, 2017, Science Translational Medicine.

Statistical strategies for microRNAseq batch effect reduction.

Yan Guo, Yu Shyr, Fei Ye, 2014, Translational cancer research.

Improvements and impacts of GRCh38 human reference on high throughput sequencing data analysis.

Yan Guo, Yu Shyr, David C Samuels, 2017, Genomics.