| 597 | -- | 600 | Balamurugan Palanisamy, Rajasekaran Ekambaram, Klaus Heese. Plasmodium falciparum 3D7 |
| 601 | -- | 605 | Douglas D. Baumann, Rebecca W. Doerge. Robust adjustment of sequence tag abundance |
| 606 | -- | 613 | Franziska Zickmann, Martin S. Lindner, Bernhard Y. Renard. GIIRA - RNA-Seq driven gene finding incorporating ambiguous reads |
| 614 | -- | 620 | Jiajie Zhang, Kassian Kobert, Tomás Flouri, Alexandros Stamatakis. PEAR: a fast and accurate Illumina Paired-End reAd mergeR |
| 621 | -- | 628 | Yue Li, Anna Goldenberg, Ka Chun Wong, Zhaolei Zhang. A probabilistic approach to explore human miRNA targetome by integrating miRNA-overexpression data and sequence information |
| 629 | -- | 635 | Luis M. Rodriguez-R, Konstantinos T. Konstantinidis. Nonpareil: a redundancy-based approach to assess the level of coverage in metagenomic datasets |
| 636 | -- | 643 | Matthew Levinson, Qing Zhou. A penalized Bayesian approach to predicting sparse protein-DNA binding landscapes |
| 644 | -- | 651 | Phuong Dao, Ibrahim Numanagic, Yen-Yi Lin, Faraz Hach, Emre Karakoç, Nilgun Donmez, Colin Collins, Evan E. Eichler, Süleyman Cenk Sahinalp. ORMAN: Optimal resolution of ambiguous RNA-Seq multimappings in the presence of novel isoforms |
| 652 | -- | 659 | Hongseok Tae, Dong-Yun Kim, John McCormick, Robert E. Settlage, Harold R. Garner. Discretized Gaussian mixture for genotyping of microsatellite loci containing homopolymer runs |
| 660 | -- | 667 | Dong Xu, Lukasz Jaroszewski, Zhanwen Li, Adam Godzik. FFAS-3D: improving fold recognition by including optimized structural features and template re-ranking |
| 668 | -- | 674 | Giuseppe Maccari, Giulia L. B. Spampinato, Valentina Tozzini. SecStAnT: secondary structure analysis tool for data selection, statistics and models building |
| 675 | -- | 681 | Ben-teng, Ting Huang, Zengyou He. Decoy-free protein-level false discovery rate estimation |
| 682 | -- | 689 | David A. Liebner, Kun Huang, Jeffrey D. Parvin. MMAD: microarray microdissection with analysis of differences is a computational tool for deconvoluting cell type-specific contributions from tissue samples |
| 690 | -- | 697 | Marina Evangelou, Frank Dudbridge, Lorenz Wernisch. Two novel pathway analysis methods based on a hierarchical model |
| 698 | -- | 705 | Emily Rose Holzinger, Scott M. Dudek, Alex T. Frase, Sarah A. Pendergrass, Marylyn D. Ritchie. ATHENA: the analysis tool for heritable and environmental network associations |
| 706 | -- | 711 | Tomomi Ichimiya, Shoko Nishihara, Sayaka Takase-Yoden, Hiroshi Kida, Kiyoko F. Aoki-Kinoshita. Frequent glycan structure mining of influenza virus data revealed a sulfated glycan motif that increased viral infection |
| 712 | -- | 718 | Joseph Geraci, Moyez Dharsee, Paulo A. S. Nuin, Alexandria Haslehurst, Madhuri Koti, Harriet E. Feilotter, Ken Evans. Exploring high dimensional data with Butterfly: a novel classification algorithm based on discrete dynamical systems |
| 719 | -- | 725 | Robert Hoehndorf, Tanya Hiebert, Nigel W. Hardy, Paul N. Schofield, Georgios V. Gkoutos, Michel Dumontier. Mouse model phenotypes provide information about human drug targets |
| 726 | -- | 733 | Johannes Stegmaier, Maryam Shahid, Masanari Takamiya, Lixin Yang, Sepand Rastegar, Markus Reischl, Uwe Strähle, Ralf Mikut. Automated prior knowledge-based quantification of neuronal patterns in the spinal cord of zebrafish |
| 734 | -- | 736 | Ole Kristian Ekseth, Martin Kuiper, Vladimir Mironov. orthAgogue: an agile tool for the rapid prediction of orthology relations |
| 737 | -- | 739 | Haoqi Sun, Haiping Wang, Ruixin Zhu, Kailin Tang, Qin Gong, Juan Cui, Zhiwei Cao, Qi Liu. iPEAP: integrating multiple omics and genetic data for pathway enrichment analysis |
| 740 | -- | 742 | Sébastien Harispe, Sylvie Ranwez, Stefan Janaqi, Jacky Montmain. The semantic measures library and toolkit: fast computation of semantic similarity and relatedness using biomedical ontologies |
| 743 | -- | 745 | Eric C. Anderson, Thomas C. Ng. Comment on 'Bayesian parentage analysis with systematic accountability of genotyping error, missing data and false matching' |