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ORCIDBMC Bioinformatics, Volume 19
Volume 19, Number 1, December 2018
- Anna Marco-Ramell, Magali Palau-Rodriguez, Ania Alay
, Sara Tulipani, Mireia Urpi-Sarda, Alex Sánchez-Pla, Cristina Andres-Lacueva:
Evaluation and comparison of bioinformatic tools for the enrichment analysis of metabolomics data. 1:1-1:11
- Min Shi, David M. Umbach, Alison S. Wise, Clarice R. Weinberg:
Simulating autosomal genotypes with realistic linkage disequilibrium and a spiked-in genetic effect. 2:1-2:10 - Peng Guo, Bo Zhu, Hong Niu, Zezhao Wang, Yonghu Liang, Yan Chen, Lupei Zhang, Hemin Ni, Yong Guo, El Hamidi A. Hay, Xue Gao, Huijiang Gao, Xiaolin Wu, Lingyang Xu, Junya Li:
Fast genomic prediction of breeding values using parallel Markov chain Monte Carlo with convergence diagnosis. 3:1-3:11 - Jader M. Caldonazzo Garbelini, André Yoshiaki Kashiwabara, Danilo Sipoli Sanches:
Sequence motif finder using memetic algorithm. 4:1-4:13 - Aditya Deshpande, Wenhua Lang, Tina McDowell, Smruthy Sivakumar, Jiexin Zhang, Jing Wang, F. Anthony San Lucas, Jerry Fowler, Humam Kadara, Paul Scheet:
Strategies for identification of somatic variants using the Ion Torrent deep targeted sequencing platform. 5:1-5:10 - Qin Zhu, Stephen A. Fisher, Hannah Dueck, Sarah Middleton, Mugdha Khaladkar, Junhyong Kim:
PIVOT: platform for interactive analysis and visualization of transcriptomics data. 6:1-6:8 - Miguel Ángel Rodríguez-García, Robert Hoehndorf:
Inferring ontology graph structures using OWL reasoning. 7:1-7:9 - Qi-Lei Zou, Xiao-Ping You, Jian-Long Li, Wing Kam Fung, Ji-Yuan Zhou:
A powerful parent-of-origin effects test for qualitative traits on X chromosome in general pedigrees. 8:1-8:9 - Min Wang, Zachary B. Abrams, Steven M. Kornblau, Kevin R. Coombes:
Thresher: determining the number of clusters while removing outliers. 9:1-9:15 - Yichen Zheng, Axel Janke:
Gene flow analysis method, the D-statistic, is robust in a wide parameter space. 10:1-10:19 - Derek S. Chiu, Aline Talhouk:
diceR: an R package for class discovery using an ensemble driven approach. 11:1-11:4 - Marek Palkowski, Wlodzimierz Bielecki:
Tuning iteration space slicing based tiled multi-core code implementing Nussinov's RNA folding. 12:1-12:12 - Audrey Legendre, Eric Angel, Fariza Tahi:
Bi-objective integer programming for RNA secondary structure prediction with pseudoknots. 13:1-13:15 - Yanhua Qiao, Yi Xiong, Hongyun Gao, Xiaolei Zhu, Peng Chen:
Protein-protein interface hot spots prediction based on a hybrid feature selection strategy. 14:1-14:16 - Juan Miguel Cejuela, Shrikant Vinchurkar, Tatyana Goldberg, Madhukar Sollepura Prabhu Shankar, Ashish Baghudana, Aleksandar Bojchevski, Carsten Uhlig, André Ofner, Pandu Raharja-Liu, Lars Juhl Jensen, Burkhard Rost:
LocText: relation extraction of protein localizations to assist database curation. 15:1-15:11 - Shifu Chen, Tanxiao Huang, Tiexiang Wen, Hong Li, Mingyan Xu, Jia Gu:
MutScan: fast detection and visualization of target mutations by scanning FASTQ data. 16:1-16:11 - Michail Tsagris, Vincenzo Lagani, Ioannis Tsamardinos:
Feature selection for high-dimensional temporal data. 17:1-17:14 - R. Michael Sivley, Jonathan H. Sheehan, Jonathan A. Kropski, Joy D. Cogan, Timothy S. Blackwell, John A. Phillips, William S. Bush, Jens Meiler, John A. Capra:
Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia. 18:1-18:10 - Chenyue W. Hu, Hanyang Li, Amina A. Qutub:
Shrinkage Clustering: a fast and size-constrained clustering algorithm for biomedical applications. 19:1-19:11 - Thomas C. A. Hitch, Christopher J. Creevey:
Spherical: an iterative workflow for assembling metagenomic datasets. 20:1-20:8 - Kyubum Lee, Byounggun Kim, Yonghwa Choi, Sunkyu Kim, Won-Ho Shin, Sunwon Lee, Sungjoon Park, Seongsoon Kim, Aik Choon Tan, Jaewoo Kang:
Deep learning of mutation-gene-drug relations from the literature. 21:1-21:13 - Badri Adhikari, Jianlin Cheng:
CONFOLD2: improved contact-driven ab initio protein structure modeling. 22:1-22:5 - Guido Zampieri, Dinh Tran-Van, Michele Donini, Nicolò Navarin, Fabio Aiolli, Alessandro Sperduti, Giorgio Valle:
Scuba: scalable kernel-based gene prioritization. 23:1-23:12 - Roman Prytuliak, Friedhelm Pfeiffer, Bianca Habermann:
SLALOM, a flexible method for the identification and statistical analysis of overlapping continuous sequence elements in sequence- and time-series data. 24:1-24:19 - Daniel Koile, Marta Cordoba, Maximiliano de Sousa Serro, Marcelo Andres Kauffman, Patricio Yankilevich:
GenIO: a phenotype-genotype analysis web server for clinical genomics of rare diseases. 25:1-25:6 - Dang Liu, Martin Hunt, Isheng J Tsai:
Inferring synteny between genome assemblies: a systematic evaluation. 26:1-26:13 - Ana Julia Velez Rueda, Alexander Miguel Monzon, Sebastián M. Ardanaz, Luis E. Iglesias, Gustavo D. Parisi:
Large scale analysis of protein conformational transitions from aqueous to non-aqueous media. 27:1-27:10 - Dorota H. Sendorek, Cristian Caloian, Kyle Ellrott, J. Christopher Bare, Takafumi N. Yamaguchi, Adam D. Ewing, Kathleen E. Houlahan, Thea C. Norman, Adam A. Margolin, Joshua M. Stuart, Paul C. Boutros:
Germline contamination and leakage in whole genome somatic single nucleotide variant detection. 28:1-28:9 - Jianzhao Gao, Yuedong Yang, Yaoqi Zhou:
Grid-based prediction of torsion angle probabilities of protein backbone and its application to discrimination of protein intrinsic disorder regions and selection of model structures. 29:1-29:8 - Jiwen Xin, Cyrus Afrasiabi, Sebastien Lelong, Julee Adesara, Ginger Tsueng, Andrew I. Su, Chunlei Wu:
Cross-linking BioThings APIs through JSON-LD to facilitate knowledge exploration. 30:1-30:7 - David E. Condon, Phu V. Tran, Yu-Chin Lien, Jonathan Schug, Michael K. Georgieff, Rebecca A. Simmons, Kyoung-Jae Won:
Defiant: (DMRs: easy, fast, identification and ANnoTation) identifies differentially Methylated regions from iron-deficient rat hippocampus. 31:1-31:12 - Eliot C. Bush, Anne E. Clark, Carissa A. DeRanek, Alexander Eng, Juliet Forman, Kevin N. Heath, Alexander B. Lee, Daniel M. Stoebel, Zunyan Wang, Matthew Wilber, Helen Wu:
xenoGI: reconstructing the history of genomic island insertions in clades of closely related bacteria. 32:1-32:11 - Billy Chiu, Sampo Pyysalo, Ivan Vulic, Anna Korhonen:
Bio-SimVerb and Bio-SimLex: wide-coverage evaluation sets of word similarity in biomedicine. 33:1-33:13 - Halil Kilicoglu, Asma Ben Abacha, Yassine Mrabet, Sonya E. Shooshan, Laritza Rodriguez, Kate Masterton, Dina Demner-Fushman:
Semantic annotation of consumer health questions. 34:1-34:28 - Sebastian Daberdaku, Carlo Ferrari:
Exploring the potential of 3D Zernike descriptors and SVM for protein-protein interface prediction. 35:1-35:23 - Marco Di Salvo, Eva Pinatel, Adelfia Talà, Marco Fondi, Clelia Peano, Pietro Alifano:
G4PromFinder: an algorithm for predicting transcription promoters in GC-rich bacterial genomes based on AT-rich elements and G-quadruplex motifs. 36:1-36:11 - Jie Zhou, Bo-quan Fu:
The research on gene-disease association based on text-mining of PubMed. 37:1-37:8 - Monika Mozere, Mehmet Tekman, Jameela Kari, Detlef Bockenhauer, Robert Kleta, Horia Stanescu:
OVAS: an open-source variant analysis suite with inheritance modelling. 46:1-46:10 - Yaogong Zhang, Jiahui Liu, Xiaohu Liu, Xin Fan, YuXiang Hong, Yuan Wang, Yalou Huang, Maoqiang Xie:
Prioritizing disease genes with an improved dual label propagation framework. 47:1-47:12 - Jeremy R. Wang, James Holt, Leonard McMillan, Corbin D. Jones:
FMLRC: Hybrid long read error correction using an FM-index. 50:1-50:11 - Christopher S. Anderson, Patrick R. McCall, Harry A. Stern, Hongmei Yang, David J. Topham:
Antigenic cartography of H1N1 influenza viruses using sequence-based antigenic distance calculation. 51:1-51:11 - Mario Latendresse, Peter D. Karp:
Evaluation of reaction gap-filling accuracy by randomization. 53:1-53:13 - Raza-Ur Rahman, Abhivyakti Gautam, Jörn Bethune, Abdul Sattar, Maksims Fiosins, Daniel Sumner Magruder, Vincenzo Capece, Orr Shomroni, Stefan Bonn:
Oasis 2: improved online analysis of small RNA-seq data. 54:1-54:10 - Raúl Arias-Carrasco, Yessenia Vásquez-Morán, Helder I. Nakaya, Vinicius Maracaja-Coutinho:
StructRNAfinder: an automated pipeline and web server for RNA families prediction. 55:1-55:7 - Pedro S. T. Russo, Gustavo R. Ferreira, Lucas E. Cardozo, Matheus C. Bürger, Raúl Arias-Carrasco, Sandra R. Maruyama, Thiago D. C. Hirata, Diógenes S. Lima, Fernando M. Passos, Kiyoshi F. Fukutani, Melissa Lever, João S. Silva, Vinicius Maracaja-Coutinho, Helder I. Nakaya:
CEMiTool: a Bioconductor package for performing comprehensive modular co-expression analyses. 56:1-56:13 - Steven Flygare, Edgar Javier Hernandez, Lon Phan, Barry Moore, Man Li, Anthony Fejes, Hao Hu, Karen Eilbeck, Chad D. Huff, Lynn Jorde, Martin G. Reese, Mark Yandell:
The VAAST Variant Prioritizer (VVP): ultrafast, easy to use whole genome variant prioritization tool. 57:1-57:13 - Oliviero Carugo:
How large B-factors can be in protein crystal structures. 61:1-61:9 - Faliu Yi, Lin Yang, Shidan Wang, Lei Guo, Chenglong Huang, Yang Xie, Guanghua Xiao:
Microvessel prediction in H&E Stained Pathology Images using fully convolutional neural networks. 64:1-64:9 - Muluye E. Liku, Elizabeth-Ann Legere, Alan M. Moses:
NoLogo: a new statistical model highlights the diversity and suggests new classes of Crm1-dependent nuclear export signals. 65:1-65:15 - César Domínguez, Jónathan Heras, Eloy J. Mata, Vico Pascual:
DecoFungi: a web application for automatic characterisation of dye decolorisation in fungal strains. 66:1-66:4 - Diego Garrido-Martín, Florencio Pazos:
Effect of the sequence data deluge on the performance of methods for detecting protein functional residues. 67:1-67:9 - Andrey Ziyatdinov, Miquel Vázquez-Santiago, Helena Brunel, Angel Martinez-Perez, Hugues Aschard, José Manuel Soria:
lme4qtl: linear mixed models with flexible covariance structure for genetic studies of related individuals. 68:1-68:5 - Amna Klich, Catherine Mercier, Laurent Gerfault, Pierre Grangeat, Corinne Beaulieu, Elodie Degout-Charmette, Tanguy Fortin, Pierre Mahé, Jean-François Giovannelli, Jean-Philippe Charrier, Audrey Giremus, Delphine Maucort-Boulch, Pascal Roy:
Variance component analysis to assess protein quantification in biomarker validation: application to selected reaction monitoring-mass spectrometry. 73:1-73:12 - Weibo Wang, Wei Sun, Wei Wang, Jin Szatkiewicz:
A randomized approach to speed up the analysis of large-scale read-count data in the application of CNV detection. 74:1-74:11 - Yözen Hernández, Rocky Bernstein, Pedro E. Pagan, Levy Vargas, William McCaig, Girish Ramrattan, Saymon Akther, Amanda Larracuente, Lia Di, Filipe G. Vieira, Wei-Gang Qiu:
BpWrapper: BioPerl-based sequence and tree utilities for rapid prototyping of bioinformatics pipelines. 76:1-76:7 - Samuel J. Yang, Marc Berndl, D. Michael Ando, Mariya Barch, Arunachalam Narayanaswamy, Eric Christiansen, Stephan Hoyer, Chris Roat, Jane Hung, Curtis T. Rueden, Asim Shankar, Steven Finkbeiner, Philip Nelson:
Assessing microscope image focus quality with deep learning. 77:1-77:9 - Regina Brinster, Anna Köttgen, Bamidele O. Tayo, Martin Schumacher, Peggy Sekula:
Control procedures and estimators of the false discovery rate and their application in low-dimensional settings: an empirical investigation. 78:1-78:10 - Skylar W. Marvel, Kimberly To, Fabian A. Grimm, Fred A. Wright, Ivan Rusyn, David M. Reif:
ToxPi Graphical User Interface 2.0: Dynamic exploration, visualization, and sharing of integrated data models. 80:1-80:7 - Jalal K. Siddiqui, Elizabeth Baskin, Mingrui Liu, Carmen Z. Cantemir-Stone, Bofei Zhang, Russell Bonneville, Joseph P. McElroy, Kevin R. Coombes, Ewy A. Mathé:
IntLIM: integration using linear models of metabolomics and gene expression data. 81:1-81:12 - Luan Lin, Wilson H. McKerrow, Bryce Richards, Chukiat Phonsom, Charles E. Lawrence:
Characterization and visualization of RNA secondary structure Boltzmann ensemble via information theory. 82:1-82:10 - Armen Abnousi, Shira L. Broschat, Ananth Kalyanaraman:
Alignment-free clustering of large data sets of unannotated protein conserved regions using minhashing. 83:1-83:18 - Varsha D. Badal, Petras J. Kundrotas, Ilya A. Vakser:
Natural language processing in text mining for structural modeling of protein complexes. 84:1-84:10 - Crhisllane Rafaele dos Santos Vasconcelos, Tulio de Lima Campos, Antônio M. Rezende:
Building protein-protein interaction networks for Leishmania species through protein structural information. 85:1-85:13 - Shuxiang Ruan, Gary D. Stormo:
Comparison of discriminative motif optimization using matrix and DNA shape-based models. 86:1-86:8 - W. Garrett Jenkinson, Jordi Abante, Andrew P. Feinberg, John Goutsias:
An information-theoretic approach to the modeling and analysis of whole-genome bisulfite sequencing data. 87:1-87:23 - Bin Zou, Victor H. F. Lee, Hong Yan:
Prediction of sensitivity to gefitinib/erlotinib for EGFR mutations in NSCLC based on structural interaction fingerprints and multilinear principal component analysis. 88:1-88:13 - Rajiv Gandhi Govindaraj, Michal Brylinski:
Comparative assessment of strategies to identify similar ligand-binding pockets in proteins. 91:1-91:17 - Haowen Zhang, Yuandong Chan, Kaichao Fan, Bertil Schmidt, Weiguo Liu:
Fast and efficient short read mapping based on a succinct hash index. 92:1-92:14 - Jesse M. Zhang, Jue Fan, H. Christina Fan, David Rosenfeld, David N. C. Tse:
An interpretable framework for clustering single-cell RNA-Seq datasets. 93:1-93:12 - Hans-Michael Müller, Kimberly Van Auken, Yuling Li, Paul W. Sternberg:
Textpresso Central: a customizable platform for searching, text mining, viewing, and curating biomedical literature. 94:1-94:16 - Gen Li, Dereje Jima, Fred A. Wright, Andrew B. Nobel:
HT-eQTL: integrative expression quantitative trait loci analysis in a large number of human tissues. 95:1-95:11 - Shu Yang, Junwen Wang, Raymond T. Ng:
Inferring RNA sequence preferences for poorly studied RNA-binding proteins based on co-evolution. 96:1-96:12 - Michael Kluge, Caroline C. Friedel:
Watchdog - a workflow management system for the distributed analysis of large-scale experimental data. 97:1-97:13 - Thomas Kovac, Tom Haber, Frank Van Reeth, Niel Hens:
Heterogeneous computing for epidemiological model fitting and simulation. 101:1-101:11 - Xilun Xiang, Haiguang Liu:
IDPM: an online database for ion distribution in protein molecules. 102:1-102:12 - Lei Huang, Li Liao, Cathy H. Wu:
Completing sparse and disconnected protein-protein network by deep learning. 103:1-103:12 - Katrijn Van Deun, Elise A. V. Crompvoets, Eva Ceulemans:
Obtaining insights from high-dimensional data: sparse principal covariates regression. 104:1-104:13 - Ingo Bulla, Benoît Aliaga, Virginia Lacal, Jan Bulla, Christoph Grunau, Cristian Chaparro:
Notos - a galaxy tool to analyze CpN observed expected ratios for inferring DNA methylation types. 105:1-105:13 - Christine Sinoquet:
A method combining a random forest-based technique with the modeling of linkage disequilibrium through latent variables, to run multilocus genome-wide association studies. 106:1-106:24 - Kun Liang, Chuanlong Du, Hankun You, Dan Nettleton:
A hidden Markov tree model for testing multiple hypotheses corresponding to Gene Ontology gene sets. 107:1-107:11 - Angel Mojarro, Julie Hachey, Gary Ruvkun, Maria T. Zuber, Christopher E. Carr:
CarrierSeq: a sequence analysis workflow for low-input nanopore sequencing. 108:1-108:4 - Peihua Chen, Chuandi Pan:
Diabetes classification model based on boosting algorithms. 109:1-109:9 - Douglas G. Howe:
A statistical approach to identify, monitor, and manage incomplete curated data sets. 110:1-110:12 - Kevin Yu Yuan Huang, Yan-Jiun Huang, Pao-Yang Chen:
BS-Seeker3: ultrafast pipeline for bisulfite sequencing. 111:1-111:4 - Anurag Verma, Yukiko Bradford, Scott M. Dudek, Anastasia Lucas, Shefali S. Verma, Sarah A. Pendergrass, Marylyn D. Ritchie:
A simulation study investigating power estimates in phenome-wide association studies. 120:1-120:8 - Braden Katzman, Doris Tang, Anthony Santella, Zhirong Bao:
AceTree: a major update and case study in the long term maintenance of open-source scientific software. 121:1-121:7 - Clemens L. Weiß, Marina Pais, Liliana M. Cano, Sophien Kamoun, Hernán A. Burbano:
nQuire: a statistical framework for ploidy estimation using next generation sequencing. 122:1-122:8 - Katarína Furmanová, Jan Byska, M. Eduard Gröller, Ivan Viola, Jan J. Palecek, Barbora Kozlíková:
COZOID: contact zone identifier for visual analysis of protein-protein interactions. 125:1-125:17 - M. Heath Farris, Andrew R. Scott, Pamela A. Texter, Marta Bartlett, Patricia Coleman, David Masters:
TIA: algorithms for development of identity-linked SNP islands for analysis by massively parallel DNA sequencing. 126:1-126:13 - Thomas Thorne:
Approximate inference of gene regulatory network models from RNA-Seq time series data. 127:1-127:12 - Nishith Kumar, Md. Aminul Hoque, Masahiro Sugimoto:
Robust volcano plot: identification of differential metabolites in the presence of outliers. 128:1-128:11 - Pathima Nusrath Hameed, Karin Verspoor, Snezana Kusljic, Saman K. Halgamuge:
A two-tiered unsupervised clustering approach for drug repositioning through heterogeneous data integration. 129:1-129:18 - Ali Oghabian, Dario Greco, Mikko J. Frilander:
IntEREst: intron-exon retention estimator. 130:1-130:10 - Senthil B. Girimurugan, Yuhang Liu, Pei-Yau Lung, Daniel L. Vera, Jonathan H. Dennis, Hank W. Bass, Jinfeng Zhang:
iSeg: an efficient algorithm for segmentation of genomic and epigenomic data. 131:1-131:15 - Jonathan Mercier, Adrien Josso, Claudine Médigue, David Vallenet:
GROOLS: reactive graph reasoning for genome annotation through biological processes. 132:1-132:12 - M. Sivade Dumousseau, Maximilian Koch, Anjali Shrivastava, Diego Alonso-López, Javier De Las Rivas, Noemi del-Toro, Colin W. Combe, Birgit H. M. Meldal, Joshua Heimbach, Juri Rappsilber, Julie M. Sullivan, Yo Yehudi, Sandra E. Orchard:
JAMI: a Java library for molecular interactions and data interoperability. 133:1-133:9 - M. Sivade Dumousseau, Diego Alonso-López, Mais G. Ammari, Glyn Bradley, Nancy H. Campbell, Arnaud Céol, Gianni Cesareni, Colin W. Combe, Javier De Las Rivas, Noemi del-Toro, Joshua Heimbach, Henning Hermjakob, Igor Jurisica, Maximilian Koch, Luana Licata, Ruth C. Lovering, David J. Lynn, Birgit H. M. Meldal, Gos Micklem, Simona Panni, Pablo Porras, Sylvie Ricard-Blum, Bernd Roechert, Lukasz Salwínski, Anjali Shrivastava, Julie M. Sullivan, Nicolas Thierry-Mieg, Yo Yehudi, Kim Van Roey, Sandra E. Orchard:
Encompassing new use cases - level 3.0 of the HUPO-PSI format for molecular interactions. 134:1-134:8 - MacIntosh Cornwell, Mahesh Vangala, Len Taing, Zachary Herbert, Johannes Köster, Bo Li, Hanfei Sun, Taiwen Li, Jian Zhang, Xintao Qiu, Matthew Pun, Rinath Jeselsohn, Myles Brown, Xiaole Shirley Liu, Henry W. Long:
VIPER: Visualization Pipeline for RNA-seq, a Snakemake workflow for efficient and complete RNA-seq analysis. 135:1-135:14 - Makbule Gulcin Ozsoy, Tansel Özyer, Faruk Polat, Reda Alhajj:
Realizing drug repositioning by adapting a recommendation system to handle the process. 136:1-136:14 - Vincent Picaud, Jean-François Giovannelli, Caroline Truntzer, Jean-Philippe Charrier, Audrey Giremus, Pierre Grangeat, Catherine Mercier:
Linear MALDI-ToF simultaneous spectrum deconvolution and baseline removal. 123:1-123:20 - Yoshihiro Noguchi, Anri Ueno, Manami Otsubo, Hayato Katsuno, Ikuto Sugita, Yuta Kanematsu, Aki Yoshida, Hiroki Esaki, Tomoya Tachi, Hitomi Teramachi:
A simple method for exploring adverse drug events in patients with different primary diseases using spontaneous reporting system. 124:1-124:7 - Martin Modrák, Jirí Vohradský:
Genexpi: a toolset for identifying regulons and validating gene regulatory networks using time-course expression data. 137:1-137:9 - Matthew D. King, Thomas Long, Daniel L. Pfalmer, Timothy L. Andersen, Owen M. McDougal:
SPIDR: small-molecule peptide-influenced drug repurposing. 138:1-138:11 - Yingxue Ren, Joseph S. Reddy, Cyril Pottier, Vivekananda Sarangi, Shulan Tian, Jason P. Sinnwell, Shannon K. McDonnell, Joanna M. Biernacka, Minerva M. Carrasquillo, Owen A. Ross, Nilüfer Ertekin-Taner, Rosa Rademakers, Matthew Hudson, Liudmila Sergeevna Mainzer, Yan W. Asmann:
Identification of missing variants by combining multiple analytic pipelines. 139:1-139:12 - Haochen Zhao, Linai Kuang, Lei Wang, Pengyao Ping, Zhanwei Xuan, Tingrui Pei, Zhelun Wu:
Prediction of microRNA-disease associations based on distance correlation set. 141:1-141:14 - Ajayrama Kumaraswamy, Kazuki Kai, Hiroyuki Ai, Hidetoshi Ikeno, Thomas Wachtler:
Spatial registration of neuron morphologies based on maximization of volume overlap. 143:1-143:16 - Christos Maramis, Athanasios Gkoufas, Anna Vardi, Evangelia Stalika, Kostas Stamatopoulos, Anastasia Hatzidimitriou, Nicos Maglaveras, Ioanna Chouvarda:
IRProfiler - a software toolbox for high throughput immune receptor profiling. 144:1-144:11 - Zhentang Li, Yi Wang, Fei Wang:
A study on fast calling variants from next-generation sequencing data using decision tree. 145:1-145:14 - Wenzhi Mao, Tong Wang, Wenxuan Zhang, Haipeng Gong:
Identification of residue pairing in interacting β-strands from a predicted residue contact map. 146:1-146:19