Dan An
5 Papers
Dan An is an academic researcher. The author has contributed to research in topics: Biology & Internal medicine. The author has an hindex of 2, co-authored 2 publications.
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Papers
cPAS-based sequencing on the BGISEQ-500 to explore small non-coding RNAs
Tobias Fehlmann,Stefanie Reinheimer,Geng Chunyu,Su Xiaoshan,Snezana Drmanac,Andrei Alexeev,Zhang Chunyan,Christina Backes,Nicole Ludwig,Martin Hart,Dan An,Zhenzhen Zhu,Chongjun Xu,Ao Chen,Ming Ni,Jian Liu,Yuxiang Li,Matthew Poulter,Yongping Li,Cord F. Stähler,Radoje Drmanac,Xun Xu,Eckart Meese,Andreas Keller +23 more
TL;DR: While there is apparently no ideal platform for all challenges of miRNome analyses, cPAS shows high technical reproducibility and supplements the hitherto available platforms.
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Exploring the role of tumor stemness and the potential of stemness-related risk model in the prognosis of intrahepatic cholangiocarcinoma
TL;DR: In this article , the role of tumor stemness in intrahepatic cholangiocarcinoma (iCCA) was explored and a prognostic risk model was established for prognosis prediction and clinical treatment guidance in iCCA patients.
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Long non-coding RNA SLC7A11 antisense RNA1 promotes oral squamous cell carcinoma progression by regulating ubiquitination of K-homology type splicing regulatory protein
TL;DR: Functionally, knockdown of SLC7A11-AS1 reduced the proliferation, migration, and invasion of oral squamous cell carcinoma cells in vitro and inhibited tumor growth as well as metastasis in vivo and is a potential therapeutic target for oral cancer.
2
Impact of sequencing depth and technology on de novo RNA-Seq assembly
Jordan Patterson,Eric J. Carpenter,Zhenzhen Zhu,Dan An,Xinming Liang,Geng Chunyu,Radoje Drmanac,Gane Ka-Shu Wong +7 more
TL;DR: Increasing sequencing depth beyond modest data sets of less than 10 Gbp recovers a plethora of single-exon transcripts undocumented in genome annotations and proves DNBseq™ is a viable alternative to HiSeq for de novo RNA-Seq assembly.
Construction and validation of molecular subtypes of coronary artery disease based on ferroptosis-related genes
TL;DR: Wang et al. as discussed by the authors constructed a reliable diagnostic model for coronary artery disease (CAD) patients and explore its potential mechanism by consensus molecular subtypes of ferroptosis-related genes.