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| Nattestad M, Goodwin S, Ng K, et al. (2018) Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line. Genome Research |
| Sedlazeck FJ, Rescheneder P, Smolka M, et al. (2018) Accurate detection of complex structural variations using single-molecule sequencing. Nature Methods |
| Fang H, Huang YF, Radhakrishnan A, et al. (2018) Scikit-ribo Enables Accurate Estimation and Robust Modeling of Translation Dynamics at Codon Resolution. Cell Systems |
| Vurture GW, Sedlazeck FJ, Nattestad M, et al. (2017) GenomeScope: Fast reference-free genome profiling from short reads. Bioinformatics (Oxford, England) |
| Fang H, Wu Y, Yang H, et al. (2017) Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine. Bmc Medical Genomics. 10: 10 |
| Fang H, Bergmann EA, Arora K, et al. (2016) Indel variant analysis of short-read sequencing data with Scalpel. Nature Protocols. 11: 2529-2548 |
| Dörfel MJ, Fang H, Crain J, et al. (2016) Proteomic and genomic characterization of a yeast model for Ogden syndrome. Yeast (Chichester, England) |
| Pan X, Lin D, Zheng Y, et al. (2016) Biodegradation of DDT by Stenotrophomonas sp. DDT-1: Characterization and genome functional analysis. Scientific Reports. 6: 21332 |
| Cheng C, Zhou Y, Li H, et al. (2016) Whole-Genome Sequencing Reveals Diverse Models of Structural Variations in Esophageal Squamous Cell Carcinoma. American Journal of Human Genetics |
| Jiménez-Barrón LT, O'Rawe JA, Wu Y, et al. (2015) Genome-wide variant analysis of simplex autism families with an integrative clinical-bioinformatics pipeline. Cold Spring Harbor Molecular Case Studies. 1: a000422 |