Fall 2019
We're meeting Fridays at 10:00 AM in the lab. Here's the schedule of journal club presentations for this semester.
Date | Person | Paper |
---|---|---|
Aug 30 | Roberto Herrera | DeNovo Congenital Heart Disease |
Sep 6 | No meeting | |
Sep 13 | Briknie Baez | Deepfinder |
Sep 20 | Luis Mieses | Gene experession |
Sep 27 | Roberto | Deep learning RNA-seq |
Oct 4 | Miguel | denoising autoencoders |
Oct 11 | BSides meeting | |
Oct 18 | No meeting | |
Oct 25 | Briknie | seq-seq-pan |
Papers
- DeNovo Congenital Heart Disease
- Zaidi, Samir, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D. Overton, Angela Romano-Adesman et al. "De novo mutations in histone-modifying genes in congenital heart disease." Nature 498, no. 7453 (2013): 220. https://www.nature.com/doifinder/10.1038/nature12141
- Axolotl
- Stewart R, Rascón CA, Tian S, Nie J, Barry C, et al. (2013). Comparative RNA-seq Analysis in the Unsequenced Axolotl: The Oncogene Burst Highlights Early Gene Expression in the Blastema. PLOS Computational Biology 9(3): e1002936. https://doi.org/10.1371/journal.pcbi.1002936
- Deepfinder
- Nung Kion Lee, Farah Liyana Azizan, Yu Shiong Wong & Norshafarina Omar (2018) DeepFinder: An integration of feature-based and deep learning approach for DNA motif discovery, Biotechnology & Biotechnological Equipment, 32:3, 759-768, DOI: https://dx.doi.org/10.1080/13102818.2018.1438209
- Gene expression
- Chen, Yifei, Yi Li, Rajiv Narayan, Aravind Subramanian, and Xiaohui Xie. "Gene expression inference with deep learning." Bioinformatics 32, no. 12 (2016): 1832-1839. https://dx.doi.org/10.1093/bioinformatics/btw074
- Deep learning RNA-Seq
- Urda, Daniel, Julio Montes-Torres, Fernando Moreno, Leonardo Franco, and José M. Jerez. "Deep learning to analyze RNA-seq gene expression data." In International Work-Conference on Artificial Neural Networks, pp. 50-59. Springer, Cham, 2017. https://core.ac.uk/download/pdf/132743527.pdf
- Denoising autoencoders
- Jie Tan, Matthew Ung, Chao Cheng, and Casey S Greene. Unsupervised feature construc-tion and knowledge extraction from genome-wide assays of breast cancer with denoising autoencoders. In Pacific Symposium on Biocomputing Co-Chairs, pages 132–143. WorldScientific, 2014. https://doi.org/10.1142/9789814644730_0014
- seq-seq-pan
- Jandrasits, C., Dabrowski, P. W., Fuchs, S., & Renard, B. Y. (2018). seq-seq-pan: Building a computational pan-genome data structure on whole genome alignment. BMC genomics, 19(1), 47. https://doi.org/10.1186/s12864-017-4401-3