太阳集团tyc官方入口团队成员至今已发表SCI文章25篇，其中共同一作8篇，包括Nature、Science、Nature genetics、Nature Communications、Scientific Reports、Oncogene多种杂志，署名文章17篇，同样包括Science、Nature等多种杂志。更多SCI文献正在技术同志和客户的合作下努力创作中。以下为技术团队已发表的文章列表：

共同一作文章

Song, Y., Li, L., Ou, Y., Gao, Z.*, Li, E., Li, X., . . . Zhan, Q. (2014). Identification of genomic alterations in oesophageal squamous cell cancer. Nature, 509(7498), 91-95. doi: 10.1038/nature13176

Cao, Y., He, M., Gao, Z.*, Peng, Y., Li, Y., Li, L., . . . Ning, G. (2014). Activating hotspot L205R mutation in PRKACA and adrenal Cushing's syndrome. Science, 344(6186), 913-917. doi: 10.1126/science.1249480

Guo, G., Sun, X., Chen, C.*, Wu, S., Huang, P., Li, Z., . . . Cai, Z. (2013). Whole-genome and whole-exome sequencing of bladder cancer identifies frequent alterations in genes involved in sister chromatid cohesion and segregation. Nat Genet. doi: 10.1038/ng.2798

Cao, Y., Gao, Z.*, Li, L., Jiang, X., Shan, A., Cai, J., . . . Ning, G. (2013). Whole exome sequencing of insulinoma reveals recurrent T372R mutations in YY1. Nature Communications, 4. doi: 10.1038/ncomms3810

Li, C., Gao, Z.*, Li, F., Li, X., Sun, Y., Wang, M., . . . Wei, Q. (2015). Whole Exome Sequencing Identifies Frequent Somatic Mutations in Cell-Cell Adhesion Genes in Chinese Patients with Lung Squamous Cell Carcinoma. Sci Rep, 5, 14237. doi: 10.1038/srep14237

Zhang, L., Zhou, Y., Cheng, C., Cui, H., Cheng, L., Kong, P., Wang, J.*, . . . Cui, Y. (2015). Genomic analyses reveal mutational signatures and frequently altered genes in esophageal squamous cell carcinoma. Am J Hum Genet, 96(4), 597-611. doi: 10.1016/j.ajhg.2015.02.017

Zhao, Y., Yang, J.*, Chen, Z., Gao, Z., Zhou, F., Li, X., . . . He, J. (2014). Identification of somatic alterations in stage I lung adenocarcinomas by next-generation sequencing. Genes Chromosomes Cancer, 53(4), 289-298. doi: 10.1002/gcc.22138

Xing, R., Li, L., Chen, L., Gao, Z.*, Wang, H., Li, W., . . . Lu, Y. (2015). Copy number variations of HLA-I and activation of NKp30 pathway determine the sensitivity of gastric cancer cells to the cytotoxicity of natural killer cells. Oncogene. doi: 10.1038/onc.2015.324

署名文章

Singh, D., Chan, J. M., Zoppoli, P., Niola, F., Sullivan, R., Castano, A., . . . Iavarone, A. (2012). Transforming fusions of FGFR and TACC genes in human glioblastoma. Science, 337(6099), 1231-1235. doi: 10.1126/science.1220834

Gui, Y., Guo, G., Huang, Y., Hu, X., Tang, A., Gao, S., . . . Cai, Z. (2011). Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder. Nat Genet, 43(9), 875-878. doi: 10.1038/ng.907

Guo, G., Gui, Y., Gao, S., Tang, A., Hu, X., Huang, Y., . . . Wang, J. (2012). Frequent mutations of genes encoding ubiquitin-mediated proteolysis pathway components in clear cell renal cell carcinoma. Nat Genet, 44(1), 17-19. doi: 10.1038/ng.1014

Chen, K., Yang, D., Li, X., Sun, B., Song, F., Cao, W., . . . Hao, X. (2015). Mutational landscape of gastric adenocarcinoma in Chinese: implications for prognosis and therapy. Proc Natl Acad Sci U S A, 112(4), 1107-1112. doi: 10.1073/pnas.1422640112

Kan, Z., Zheng, H., Liu, X., Li, S., Barber, T. D., Gong, Z., . . . Mao, M. (2013). Whole-genome sequencing identifies recurrent mutations in hepatocellular carcinoma. Genome Res, 23(9), 1422-1433. doi: 10.1101/gr.154492.113

Wu, S., Huang, P., Li, C., Huang, Y., Li, X., Wang, Y., . . . Cai, Z. (2013). Telomerase Reverse Transcriptase Gene Promoter Mutations Help Discern the Origin of Urogenital Tumors: A Genomic and Molecular Study. Eur Urol. doi: 10.1016/j.eururo.2013.10.038

Jhunjhunwala, S., Jiang, Z., Stawiski, E. W., Gnad, F., Liu, J., Mayba, O., . . . Zhang, Z. (2014). Diverse modes of genomic alteration in hepatocellular carcinoma. Genome Biol, 15(8), 436. doi: 10.1186/s13059-014-0436-9

Lou, S., Lee, H. M., Qin, H., Li, J. W., Gao, Z., Liu, X., . . . Yip, K. Y. (2014). Whole-genome bisulfite sequencing of multiple individuals reveals complementary roles of promoter and gene body methylation in transcriptional regulation. Genome Biol, 15(7), 408. doi: 10.1186/s13059-014-0408-0

Cai, J., Li, L., Ye, L., Jiang, X., Shen, L., Gao, Z., . . . Ning, G. (2015). Exome sequencing reveals mutant genes with low penetrance involved in MEN2A-associated tumorigenesis. Endocr Relat Cancer, 22(1), 23-33. doi: 10.1530/ERC-14-0225

de Miranda, N. F., Georgiou, K., Chen, L., Wu, C., Gao, Z., Zaravinos, A., . . . Pan-Hammarstrom, Q. (2014). Exome sequencing reveals novel mutation targets in diffuse large B-cell lymphomas derived from Chinese patients. Blood, 124(16), 2544-2553. doi: 10.1182/blood-2013-12-546309

de Miranda, N. F., Peng, R., Georgiou, K., Wu, C., Falk Sorqvist, E., Berglund, M., . . . Pan-Hammarstrom, Q. (2013). DNA repair genes are selectively mutated in diffuse large B cell lymphomas. J Exp Med, 210(9), 1729-1742. doi: 10.1084/jem.20122842

Gao, S., Zou, D., Mao, L., Liu, H., Song, P., Chen, Y., . . . Bolund, L. (2015). BS-SNPer: SNP calling in Bisulfite-seq data. Bioinformatics. doi: 10.1093/bioinformatics/btv507

Wang, Q., Wen, B., Yan, G., Wei, J., Xie, L., Xu, S., . . . Liu, S. (2013). Qualitative and quantitative expression status of the human chromosome 20 genes in cancer tissues and the representative cell lines. J Proteome Res, 12(1), 151-161. doi: 10.1021/pr3008336

Yu, J., Wu, W. K., Li, X., He, J., Li, X. X., Ng, S. S., . . . Sung, J. J. (2015). Novel recurrently mutated genes and a prognostic mutation signature in colorectal cancer. Gut, 64(4), 636-645. doi: 10.1136/gutjnl-2013-306620

Zhou, D., Yang, L., Zheng, L., Ge, W., Li, D., Zhang, Y., . . . Zheng, S. (2013). Exome capture sequencing of adenoma reveals genetic alterations in multiple cellular pathways at the early stage of colorectal tumorigenesis. PLoS One, 8(1), e53310. doi: 10.1371/journal.pone.0053310

Hong, J. Y., Liu, X., Mao, M., Li, M., Choi, D. I., Kang, S. W., . . . La Choi, Y. (2013). Genetic aberrations in imatinib-resistant dermatofibrosarcoma protuberans revealed by whole genome sequencing. PLoS One, 8(7), e69752. doi: 10.1371/journal.pone.0069752

Wang, Y., Li, W., Xia, Y., Wang, C., Tang, Y. T., Guo, W., . . . Li, J. (2014). Identifying Human Genome-Wide CNV, LOH and UPD by Targeted Sequencing of Selected Regions. PLoS One, 10(4), e0123081. doi: 10.1371/journal.pone.0123081