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  1. Post-hybridization washing is an essential part of microarray experiments. Both the quality of the experimental washing protocol and adequate consideration of washing in intensity calibration ultimately affect...

    Authors: Hans Binder, Knut Krohn and Conrad J Burden
    Citation: BMC Bioinformatics 2010 11:291
  2. Concomitant with the rise in the popularity of DNA microarrays has been a surge of proposed methods for the analysis of microarray data. Fully controlled "spike-in" datasets are an invaluable but rare tool for...

    Authors: Qianqian Zhu, Jeffrey C Miecznikowski and Marc S Halfon
    Citation: BMC Bioinformatics 2010 11:285
  3. The incorporation of annotated sequence information from multiple related species in commonly used databases (Ensembl, Flybase, Saccharomyces Genome Database, Wormbase, etc.) has increased dramatically over th...

    Authors: Steven N Steinway, Ruth Dannenfelser, Christopher D Laucius, James E Hayes and Sudhir Nayak
    Citation: BMC Bioinformatics 2010 11:284
  4. Contact maps have been extensively used as a simplified representation of protein structures. They capture most important features of a protein's fold, being preferred by a number of researchers for the descri...

    Authors: Jose M Duarte, Rajagopal Sathyapriya, Henning Stehr, Ioannis Filippis and Michael Lappe
    Citation: BMC Bioinformatics 2010 11:283
  5. The omics fields promise to revolutionize our understanding of biology and biomedicine. However, their potential is compromised by the challenge to analyze the huge datasets produced. Analysis of omics data is...

    Authors: Martin Eklund, Ola Spjuth and Jarl ES Wikberg
    Citation: BMC Bioinformatics 2010 11:282
  6. High-throughput measurement of allele-specific expression (ASE) is a relatively new and exciting application area for array-based technologies. In this paper, we explore several data sets which make use of Ill...

    Authors: Matthew E Ritchie, Matthew S Forrest, Antigone S Dimas, Caroline Daelemans, Emmanouil T Dermitzakis, Panagiotis Deloukas and Simon Tavaré
    Citation: BMC Bioinformatics 2010 11:280
  7. Microarray technology is a powerful and widely accepted experimental technique in molecular biology that allows studying genome wide transcriptional responses. However, experimental data usually contain potent...

    Authors: Tung T Nguyen, Richard R Almon, Debra C DuBois, William J Jusko and Ioannis P Androulakis
    Citation: BMC Bioinformatics 2010 11:279
  8. Different microarray studies have compiled gene lists for predicting outcomes of a range of treatments and diseases. These have produced gene lists that have little overlap, indicating that the results from an...

    Authors: Gad Abraham, Adam Kowalczyk, Sherene Loi, Izhak Haviv and Justin Zobel
    Citation: BMC Bioinformatics 2010 11:277
  9. A major goal of the analysis of high-dimensional RNA expression data from tumor tissue is to identify prognostic signatures for discriminating patient subgroups. For this purpose genome-wide identification of ...

    Authors: Birte Hellwig, Jan G Hengstler, Marcus Schmidt, Mathias C Gehrmann, Wiebke Schormann and Jörg Rahnenführer
    Citation: BMC Bioinformatics 2010 11:276
  10. Tiling-arrays are applicable to multiple types of biological research questions. Due to its advantages (high sensitivity, resolution, unbiased), the technology is often employed in genome-wide investigations. ...

    Authors: Erdogan Taskesen, Renee Beekman, Jeroen de Ridder, Bas J Wouters, Justine K Peeters, Ivo P Touw, Marcel JT Reinders and Ruud Delwel
    Citation: BMC Bioinformatics 2010 11:275
  11. Current imaging methods such as Magnetic Resonance Imaging (MRI), Confocal microscopy, Electron Microscopy (EM) or Selective Plane Illumination Microscopy (SPIM) yield three-dimensional (3D) data sets in need ...

    Authors: Benjamin Schmid, Johannes Schindelin, Albert Cardona, Mark Longair and Martin Heisenberg
    Citation: BMC Bioinformatics 2010 11:274
  12. Most of the existing in silico phosphorylation site prediction systems use machine learning approach that requires preparing a good set of classification data in order to build the classification knowledge. Furth...

    Authors: Ashis Kumer Biswas, Nasimul Noman and Abdur Rahman Sikder
    Citation: BMC Bioinformatics 2010 11:273
  13. Large-scale genomic studies often identify large gene lists, for example, the genes sharing the same expression patterns. The interpretation of these gene lists is generally achieved by extracting concepts ove...

    Authors: Xin He, Moushumi Sen Sarma, Xu Ling, Brant Chee, Chengxiang Zhai and Bruce Schatz
    Citation: BMC Bioinformatics 2010 11:272
  14. Next-generation amplicon sequencing enables high-throughput genetic diagnostics, sequencing multiple genes in several patients together in one sequencing run. Currently, no open-source out-of-the-box software ...

    Authors: Joachim M De Schrijver, Kim De Leeneer, Steve Lefever, Nick Sabbe, Filip Pattyn, Filip Van Nieuwerburgh, Paul Coucke, Dieter Deforce, Jo Vandesompele, Sofie Bekaert, Jan Hellemans and Wim Van Criekinge
    Citation: BMC Bioinformatics 2010 11:269
  15. Typical evolutionary events like recombination, hybridization or gene transfer make necessary the use of phylogenetic networks to properly depict the evolution of DNA and protein sequences. Although several th...

    Authors: Miguel Arenas, Mateus Patricio, David Posada and Gabriel Valiente
    Citation: BMC Bioinformatics 2010 11:268
  16. Observed co-expression of a group of genes is frequently attributed to co-regulation by shared transcription factors. This assumption has led to the hypothesis that promoters of co-expressed genes should share...

    Authors: Guofeng Meng, Axel Mosig and Martin Vingron
    Citation: BMC Bioinformatics 2010 11:267
  17. High resolution mass spectrometry has been employed to rapidly and accurately type and subtype influenza viruses. The detection of signature peptides with unique theoretical masses enables the unequivocal assi...

    Authors: Jason WH Wong, Alexander B Schwahn and Kevin M Downard
    Citation: BMC Bioinformatics 2010 11:266
  18. A new paradigm of biological investigation takes advantage of technologies that produce large high throughput datasets, including genome sequences, interactions of proteins, and gene expression. The ability of...

    Authors: Troy Hawkins, Meghana Chitale and Daisuke Kihara
    Citation: BMC Bioinformatics 2010 11:265
  19. Understanding the genetic basis of disease risk in depth requires an exhaustive knowledge of the types of genetic variation. Very recently, Copy Number Variants (CNVs) have received much attention because of t...

    Authors: Arnald Alonso, Antonio Julià, Raül Tortosa, Cristina Canaleta, Juan D Cañete, Javier Ballina, Alejandro Balsa, Jesús Tornero and Sara Marsal
    Citation: BMC Bioinformatics 2010 11:264
  20. The Protein-DNA Interface database (PDIdb) is a repository containing relevant structural information of Protein-DNA complexes solved by X-ray crystallography and available at the Protein Data Bank. The databa...

    Authors: Tomás Norambuena and Francisco Melo
    Citation: BMC Bioinformatics 2010 11:262
  21. The replication rate (or fitness) between viral variants has been investigated in vivo and in vitro for human immunodeficiency virus (HIV). HIV fitness plays an important role in the development and persistence o...

    Authors: Jingming Ma, Carrie Dykes, Tao Wu, Yangxin Huang, Lisa Demeter and Hulin Wu
    Citation: BMC Bioinformatics 2010 11:261
  22. Shared-usage high throughput screening (HTS) facilities are becoming more common in academe as large-scale small molecule and genome-scale RNAi screening strategies are adopted for basic research purposes. The...

    Authors: Andrew N Tolopko, John P Sullivan, Sean D Erickson, David Wrobel, Su L Chiang, Katrina Rudnicki, Stewart Rudnicki, Jennifer Nale, Laura M Selfors, Dara Greenhouse, Jeremy L Muhlich and Caroline E Shamu
    Citation: BMC Bioinformatics 2010 11:260
  23. Large comparative genomics studies and tools are becoming increasingly more compute-expensive as the number of available genome sequences continues to rise. The capacity and cost of local computing infrastruct...

    Authors: Dennis P Wall, Parul Kudtarkar, Vincent A Fusaro, Rimma Pivovarov, Prasad Patil and Peter J Tonellato
    Citation: BMC Bioinformatics 2010 11:259
  24. MicroRNAs (miRNAs) are non-coding RNAs that regulate gene expression by binding to the messenger RNA (mRNA) of protein coding genes. They control gene expression by either inhibiting translation or inducing mR...

    Authors: Stephen F Madden, Susan B Carpenter, Ian B Jeffery, Harry Björkbacka, Katherine A Fitzgerald, Luke A O'Neill and Desmond G Higgins
    Citation: BMC Bioinformatics 2010 11:257
  25. Modelling the ligand binding site of a protein is an important component of understanding protein-ligand interactions and is being actively studied. Even if the side chains are restricted to rotamers, a set of...

    Authors: Edon Sung, Sangsoo Kim and Whanchul Shin
    Citation: BMC Bioinformatics 2010 11:256
  26. Recently there has been an explosion of new data sources about genes, proteins, genetic variations, chemical compounds, diseases and drugs. Integration of these data sources and the identification of patterns ...

    Authors: Bin Chen, Xiao Dong, Dazhi Jiao, Huijun Wang, Qian Zhu, Ying Ding and David J Wild
    Citation: BMC Bioinformatics 2010 11:255
  27. Normalization in real-time qRT-PCR is necessary to compensate for experimental variation. A popular normalization strategy employs reference gene(s), which may introduce additional variability into normalized ...

    Authors: Inna Chervoneva, Yanyan Li, Stephanie Schulz, Sean Croker, Chantell Wilson, Scott A Waldman and Terry Hyslop
    Citation: BMC Bioinformatics 2010 11:253
  28. Protein alignments are an essential tool for many bioinformatics analyses. While sequence alignments are accurate for proteins of high sequence similarity, they become unreliable as they approach the so-called...

    Authors: Florian Teichert, Jonas Minning, Ugo Bastolla and Markus Porto
    Citation: BMC Bioinformatics 2010 11:251
  29. MicroRNAs (miRNAs) are an abundant class of small noncoding RNAs (20-24 nts) that can affect gene expression by post-transcriptional regulation of mRNAs. They play important roles in several biological process...

    Authors: Isana Veksler-Lublinsky, Yonat Shemer-Avni, Klara Kedem and Michal Ziv-Ukelson
    Citation: BMC Bioinformatics 2010 11:249
  30. Several algorithms have been proposed for detecting fluorescently labeled subcellular objects in microscope images. Many of these algorithms have been designed for specific tasks and validated with limited ima...

    Authors: Pekka Ruusuvuori, Tarmo Äijö, Sharif Chowdhury, Cecilia Garmendia-Torres, Jyrki Selinummi, Mirko Birbaumer, Aimée M Dudley, Lucas Pelkmans and Olli Yli-Harja
    Citation: BMC Bioinformatics 2010 11:248
  31. DNA replication is a fundamental biological process during S phase of cell division. It is initiated from several hundreds of origins along whole chromosome with different firing efficiencies (or frequency of ...

    Authors: Huaien Luo, Juntao Li, Majid Eshaghi, Jianhua Liu and R Krishna Murthy Karuturi
    Citation: BMC Bioinformatics 2010 11:247
  32. High-throughput genotyping microarrays assess both total DNA copy number and allelic composition, which makes them a tool of choice for copy number studies in cancer, including total copy number and loss of he...

    Authors: Henrik Bengtsson, Pierre Neuvial and Terence P Speed
    Citation: BMC Bioinformatics 2010 11:245
  33. Many protein interactions, especially those involved in signaling, involve short linear motifs consisting of 5-10 amino acid residues that interact with modular protein domains such as the SH3 binding domains ...

    Authors: Hugo YK Lam, Philip M Kim, Janine Mok, Raffi Tonikian, Sachdev S Sidhu, Benjamin E Turk, Michael Snyder and Mark B Gerstein
    Citation: BMC Bioinformatics 2010 11:243
  34. The Ensembl project produces updates to its comparative genomics resources with each of its several releases per year. During each release cycle approximately two weeks are allocated to generate all the genomi...

    Authors: Jessica Severin, Kathryn Beal, Albert J Vilella, Stephen Fitzgerald, Michael Schuster, Leo Gordon, Abel Ureta-Vidal, Paul Flicek and Javier Herrero
    Citation: BMC Bioinformatics 2010 11:240
  35. The Ensembl web site has provided access to genomic information for almost 10 years. During this time the amount of data available through Ensembl has grown dramatically. At the same time, the World Wide Web i...

    Authors: Anne Parker, Eugene Bragin, Simon Brent, Bethan Pritchard, James A Smith and Stephen Trevanion
    Citation: BMC Bioinformatics 2010 11:239
  36. Advances in sequencing and genotyping technologies are leading to the widespread availability of multi-species variation data, dense genotype data and large-scale resequencing projects. The 1000 Genomes Projec...

    Authors: Daniel Rios, William M McLaren, Yuan Chen, Ewan Birney, Arne Stabenau, Paul Flicek and Fiona Cunningham
    Citation: BMC Bioinformatics 2010 11:238
  37. Protein-protein docking for proteins with large conformational changes was analyzed by using interaction fingerprints, one of the scales for measuring similarities among complex structures, utilized especially...

    Authors: Nobuyuki Uchikoga and Takatsugu Hirokawa
    Citation: BMC Bioinformatics 2010 11:236

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