301 | -- | 305 | Sankar Subramanian. Using the plurality of codon positions to identify deleterious variants in human exomes |
306 | -- | 310 | James Vlasblom, Khalid Zuberi, Harold Rodriguez, Roland Arnold, Alla Gagarinova, Viktor Deineko, Ashwani Kumar, Elisa Leung, Kamran Rizzolo, Bahram Samanfar, Luke Chang, Sadhna Phanse, Ashkan Golshani, Jack Greenblatt, Walid A. Houry, Andrew Emili, Quaid Morris, Gary D. Bader, Mohan Babu. Escherichia coli |
311 | -- | 317 | Jonathan D. Magasin, Dietlind L. Gerloff. Pooled assembly of marine metagenomic datasets: enriching annotation through chimerism |
318 | -- | 323 | Jing Wang, Leon Raskin, David C. Samuels, Yu Shyr, Yan Guo. Genome measures used for quality control are dependent on gene function and ancestry |
324 | -- | 331 | Yi-Kuo Yu, John A. Capra, Aleksandar Stojmirovic, David Landsman, Stephen F. Altschul. Log-odds sequence logos |
332 | -- | 339 | Andrzej Zielezinski, Wojciech M. Karlowski. Integrative data analysis indicates an intrinsic disordered domain character of Argonaute-binding motifs |
340 | -- | 345 | René Luijk, Jelle J. Goeman, P. Eline Slagboom, Bastiaan T. Heijmans, Erik W. van Zwet. An alternative approach to multiple testing for methylation QTL mapping reduces the proportion of falsely identified CpGs |
346 | -- | 354 | Katharina Nöh, Peter Droste, Wolfgang Wiechert. 13C-metabolic flux analysis |
355 | -- | 362 | Maria Anna Rapsomaniki, Eugenio Cinquemani, Nickolaos-Nikiforos Giakoumakis, Panagiotis Kotsantis, John Lygeros, Zoi Lygerou. Inference of protein kinetics by stochastic modeling and simulation of fluorescence recovery after photobleaching experiments |
363 | -- | 372 | Jialu Hu, Knut Reinert. conserved modules in multiple networks |
373 | -- | 381 | Ralf Schmidt, Silvio Waschina, Daniela Boettger-Schmidt, Christian Kost, Christoph Kaleta. Computing autocatalytic sets to unravel inconsistencies in metabolic network reconstructions |
382 | -- | 389 | Ralph Patrick, Kim-Anh Lê Cao, Bostjan Kobe, Mikael Bodén. PhosphoPICK: modelling cellular context to map kinase-substrate phosphorylation events |
390 | -- | 396 | Hamidreza Khataee, Alan Wee-Chung Liew. A stochastic automaton model for simulating kinesin processivity |
397 | -- | 404 | Philippe Bastien, Frédéric Bertrand, Nicolas Meyer, Myriam Maumy-Bertrand. Deviance residuals-based sparse PLS and sparse kernel PLS regression for censored data |
405 | -- | 412 | Zhihai Liu, Yan Li, Li Han, Jie Li, Jie Liu, Zhixiong Zhao, Wei Nie, Yuchen Liu, Renxiao Wang. PDB-wide collection of binding data: current status of the PDBbind database |
413 | -- | 415 | Ulrich Wittelsbürger, Bastian Pfeifer, Martin J. Lercher. WhopGenome: high-speed access to whole-genome variation and sequence data in R |
416 | -- | 417 | Ryan M. Ames, Simon C. Lovell. DupliPHY-Web: a web server for DupliPHY and DupliPHY-ML |
418 | -- | 420 | Tune H. Pers, Pascal Timshel, Joel Hirschhorn. SNPsnap: a Web-based tool for identification and annotation of matched SNPs |
421 | -- | 422 | Dina Zhabinskaya, Sally Madden, Craig J. Benham. SIST: stress-induced structural transitions in superhelical DNA |
423 | -- | 425 | Stefan Janssen, Robert Giegerich. The RNA shapes studio |
426 | -- | 428 | Zexuan Zhu, Linsen Li, Yongpeng Zhang, Yanli Yang, Xiao Yang. CompMap: a reference-based compression program to speed up read mapping to related reference sequences |
429 | -- | 431 | Javad Nadaf, Jacek Majewski, Somayyeh Fahiminiya. ExomeAI: detection of recurrent allelic imbalance in tumors using whole-exome sequencing data |
432 | -- | 433 | Ruchi Chaudhary, David Fernández-Baca, John Gordon Burleigh. MulRF: a software package for phylogenetic analysis using multi-copy gene trees |
434 | -- | 435 | Pier Paolo Olimpieri, Paolo Marcatili, Anna Tramontano. Tabhu: tools for antibody humanization |
436 | -- | 437 | Marc W. Schmid, Ueli Grossniklaus. Rcount: simple and flexible RNA-Seq read counting |
438 | -- | 439 | Giovanni Marco Dall'Olio, Ali R. Vahdati, Jaume Bertranpetit, Andreas Wagner, Hafid Laayouni. VCF2Networks: applying genotype networks to single-nucleotide variants data |
440 | -- | 441 | Heiko Giese, Jörg Ackermann, Heinrich Heide, Lea Bleier, Stefan Dröse, Ilka Wittig, Ulrich Brandt, Ina Koch. NOVA: a software to analyze complexome profiling data |
442 | -- | 444 | Avigail Taylor, Julia Steinberg, Tallulah S. Andrews, Caleb Webber. GeneNet Toolbox for MATLAB: a flexible platform for the analysis of gene connectivity in biological networks |
445 | -- | 446 | Steffen Priebe, Christian Kreisel, Fabian Horn, Reinhard Guthke, Jörg Linde. FungiFun2: a comprehensive online resource for systematic analysis of gene lists from fungal species |
447 | -- | 448 | Benjamin Linard, Alexis Allot, Raphael Schneider, Can Morel, Raymond Ripp, Marc Bigler, Julie Dawn Thompson, Olivier Poch, Odile Lecompte. OrthoInspector 2.0: Software and database updates |
449 | -- | 450 | Yana Bromberg, Emidio Capriotti. Editor's Choice: SNP-SIG 2013: the state of the art of genomic variant interpretation |