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Page 180 of 249

  1. Polymorphic variants and mutations disrupting canonical splicing isoforms are among the leading causes of human hereditary disorders. While there is a substantial evidence of aberrant splicing causing Mendelia...

    Authors: Alexander Churbanov, Igor Vořechovský and Chindo Hicks
    Citation: BMC Bioinformatics 2010 11:22
  2. De Bruijn graphs are a theoretical framework underlying several modern genome assembly programs, especially those that deal with very short reads. We describe an application of de Bruijn graphs to analyze the ...

    Authors: Carl Kingsford, Michael C Schatz and Mihai Pop
    Citation: BMC Bioinformatics 2010 11:21
  3. Theme-driven cancer survival studies address whether the expression signature of genes related to a biological process can predict patient survival time. Although this should ideally be achieved by testing two...

    Authors: Esteban Czwan, Benedikt Brors and David Kipling
    Citation: BMC Bioinformatics 2010 11:19
  4. Recent reanalysis of spike-in datasets underscored the need for new and more accurate benchmark datasets for statistical microarray analysis. We present here a fresh method using biologically-relevant data to ...

    Authors: Benoît De Hertogh, Bertrand De Meulder, Fabrice Berger, Michael Pierre, Eric Bareke, Anthoula Gaigneaux and Eric Depiereux
    Citation: BMC Bioinformatics 2010 11:17
  5. Considering energy function to detect a correct protein fold from incorrect ones is very important for protein structure prediction and protein folding. Knowledge-based mean force potentials are certainly the ...

    Authors: Shahriar Arab, Mehdi Sadeghi, Changiz Eslahchi, Hamid Pezeshk and Armita Sheari
    Citation: BMC Bioinformatics 2010 11:16
  6. A key challenge in systems biology is the reconstruction of an organism's metabolic network from its genome sequence. One strategy for addressing this problem is to predict which metabolic pathways, from a ref...

    Authors: Joseph M Dale, Liviu Popescu and Peter D Karp
    Citation: BMC Bioinformatics 2010 11:15
  7. Large datasets of protein interactions provide a rich resource for the discovery of Short Linear Motifs (SLiMs) that recur in unrelated proteins. However, existing methods for estimating the probability of mot...

    Authors: Norman E Davey, Richard J Edwards and Denis C Shields
    Citation: BMC Bioinformatics 2010 11:14
  8. Developing and evaluating new technology that enables researchers to recover gene-expression levels of colonic cells from fecal samples could be key to a non-invasive screening tool for early detection of colo...

    Authors: Nysia I George, Joanne R Lupton, Nancy D Turner, Robert S Chapkin, Laurie A Davidson and Naisyin Wang
    Citation: BMC Bioinformatics 2010 11:13
  9. The functional and s tructural characterisation of enzymes that belong to microbial metabolic pathways is very important for structure-based drug design. The main interest in studying shikimate pathway enzymes in...

    Authors: Helen A Arcuri, Geraldo FD Zafalon, Evandro A Marucci, Carlos E Bonalumi, Nelson JF da Silveira, José M Machado, Walter F de Azevedo Jr and Mário S Palma
    Citation: BMC Bioinformatics 2010 11:12
  10. Human cancer is caused by the accumulation of tumor-specific mutations in oncogenes and tumor suppressors that confer a selective growth advantage to cells. As a consequence of genomic instability and high lev...

    Authors: Jingjing Ye, Adam Pavlicek, Elizabeth A Lunney, Paul A Rejto and Chi-Hse Teng
    Citation: BMC Bioinformatics 2010 11:11
  11. Complex diseases are multifactorial traits caused by both genetic and environmental factors. They represent the major part of human diseases and include those with largest prevalence and mortality (cancer, hea...

    Authors: Roberto Amato, Michele Pinelli, Daniel D'Andrea, Gennaro Miele, Mario Nicodemi, Giancarlo Raiconi and Sergio Cocozza
    Citation: BMC Bioinformatics 2010 11:8
  12. Several bioinformatic approaches have previously been used to find novel sites of ADAR mediated A-to-I RNA editing in human. These studies have discovered thousands of genes that are hyper-edited in their non-...

    Authors: Mats Ensterö, Örjan Åkerborg, Daniel Lundin, Bei Wang, Terrence S Furey, Marie Öhman and Jens Lagergren
    Citation: BMC Bioinformatics 2010 11:6
  13. Many complementary solutions are available for the identifier mapping problem. This creates an opportunity for bioinformatics tool developers. Tools can be made to flexibly support multiple mapping services or...

    Authors: Martijn P van Iersel, Alexander R Pico, Thomas Kelder, Jianjiong Gao, Isaac Ho, Kristina Hanspers, Bruce R Conklin and Chris T Evelo
    Citation: BMC Bioinformatics 2010 11:5
  14. Sequence comparisons make use of a one-letter representation for amino acids, the necessary quantitative information being supplied by the substitution matrices. This paper deals with the problem of finding a ...

    Authors: Karel Zimmermann and Jean-François Gibrat
    Citation: BMC Bioinformatics 2010 11:4
  15. Correction to Chakrabarti S, Lanczycki CJ, Panchenko AR, Przytycka TM, Thiessen PA and Bryant SH: State of the art: refinement of multiple sequence alignments. BMC Bioinformatics 2006, 7:499.

    Authors: Saikat Chakrabarti, Christopher J Lanczycki, Anna R Panchenko, Teresa M Przytycka, Paul A Thiessen and Stephen H Bryant
    Citation: BMC Bioinformatics 2010 11:3

    The original article was published in BMC Bioinformatics 2006 7:499

  16. S. cerevisiae, A. thaliana and M. musculus are well-studied organisms in biology and the sequencing of their genomes was completed many years ago. It is still a challenge, however, to develop methods that assign ...

    Authors: Leander Schietgat, Celine Vens, Jan Struyf, Hendrik Blockeel, Dragi Kocev and Sašo Džeroski
    Citation: BMC Bioinformatics 2010 11:2
  17. Protein-protein interactions (PPIs) constitute one of the most crucial conditions to sustain life in living organisms. To study PPI in Arabidopsis thaliana we have developed AtPIN, a database and web interface...

    Authors: Marcelo M Brandão, Luiza L Dantas and Marcio C Silva-Filho
    Citation: BMC Bioinformatics 2009 10:454
  18. The increasing number of gene expression microarray studies represents an important resource in biomedical research. As a result, gene expression based diagnosis has entered clinical practice for patient strat...

    Authors: Andreas Buness, Markus Ruschhaupt, Ruprecht Kuner and Achim Tresch
    Citation: BMC Bioinformatics 2009 10:453
  19. It is increasingly evident that there are multiple and overlapping patterns within the genome, and that these patterns contain different types of information - regarding both genome function and genome history...

    Authors: Josiah D Seaman and John C Sanford
    Citation: BMC Bioinformatics 2009 10:452
  20. Some upstream open reading frames (uORFs) regulate gene expression (i.e., they are functional) and can play key roles in keeping organisms healthy. However, how uORFs are involved in gene regulation is not yet...

    Authors: Selpi, Christopher H Bryant, Graham JL Kemp, Janeli Sarv, Erik Kristiansson and Per Sunnerhagen
    Citation: BMC Bioinformatics 2009 10:451
  21. The study of biological networks has led to the development of increasingly large and detailed models. Computer tools are essential for the simulation of the dynamical behavior of the networks from the model. ...

    Authors: Pedro T Monteiro, Estelle Dumas, Bruno Besson, Radu Mateescu, Michel Page, Ana T Freitas and Hidde de Jong
    Citation: BMC Bioinformatics 2009 10:450
  22. Microarrays depend on appropriate probe design to deliver the promise of accurate genome-wide measurement. Probe design, ideally, produces a unique probe-target match with homogeneous duplex stability over the...

    Authors: Kevin J Thompson, Hrishikesh Deshmukh, Jeffrey L Solka and Jennifer W Weller
    Citation: BMC Bioinformatics 2009 10:449
  23. The decreasing costs of capillary-based Sanger sequencing and next generation technologies, such as 454 pyrosequencing, have prompted an explosion of transcriptome projects in non-model species, where even sha...

    Authors: Alexie Papanicolaou, Remo Stierli, Richard H ffrench-Constant and David G Heckel
    Citation: BMC Bioinformatics 2009 10:447
  24. Predicting the function of a protein from its sequence is a long-standing challenge of bioinformatic research, typically addressed using either sequence-similarity or sequence-motifs. We employ the novel motif...

    Authors: Uri Weingart, Yair Lavi and David Horn
    Citation: BMC Bioinformatics 2009 10:446
  25. Functional annotation of rapidly amassing nucleotide and protein sequences presents a challenging task for modern bioinformatics. This is particularly true for protein families sharing extremely low sequence i...

    Authors: Jayashree Ramana and Dinesh Gupta
    Citation: BMC Bioinformatics 2009 10:445
  26. Combining multiple independent tests, when all test the same hypothesis and in the same direction, has been the subject of several approaches. Besides the inappropriate (in this case) Bonferroni procedure, the...

    Authors: Thierry De Meeûs, Jean-François Guégan and Anatoly T Teriokhin
    Citation: BMC Bioinformatics 2009 10:443
  27. The relative preference of nucleosomes to form on individual DNA sequences plays a major role in genome packaging. A wide variety of DNA sequence features are believed to influence nucleosome formation, includ...

    Authors: Desiree Tillo and Timothy R Hughes
    Citation: BMC Bioinformatics 2009 10:442
  28. Legumes (Leguminosae or Fabaceae) play a major role in agriculture. Transcriptomics studies in the model legume species, Medicago truncatula, are instrumental in helping to formulate hypotheses about the role of ...

    Authors: Ji He, Vagner A Benedito, Mingyi Wang, Jeremy D Murray, Patrick X Zhao, Yuhong Tang and Michael K Udvardi
    Citation: BMC Bioinformatics 2009 10:441
  29. The Affymetrix MitoChip v2.0 is an oligonucleotide tiling array for the resequencing of the human mitochondrial (mt) genome. For each of 16,569 nucleotide positions of the mt genome it holds two sets of four 2...

    Authors: Marian Thieme, Claudio Lottaz, Harald Niederstätter, Walther Parson, Rainer Spang and Peter J Oefner
    Citation: BMC Bioinformatics 2009 10:440
  30. Over the last decade several prediction methods have been developed for determining the structural and functional properties of individual protein residues using sequence and sequence-derived information. Most...

    Authors: Huzefa Rangwala, Christopher Kauffman and George Karypis
    Citation: BMC Bioinformatics 2009 10:439
  31. For gene expression data obtained from a time-course microarray experiment, Liu et al. [1] developed a new algorithm for clustering genes with similar expression profiles over time. Performance of their proposal ...

    Authors: Shyamal D Peddada, David M Umbach and Shawn F Harris
    Citation: BMC Bioinformatics 2009 10:438
  32. Prediction of transcriptional regulatory mechanisms in Arabidopsis has become increasingly critical with the explosion of genomic data now available for both gene expression and gene sequence composition. We have...

    Authors: Damion Nero, Manpreet S Katari, Jonathan Kelfer, Daniel Tranchina and Gloria M Coruzzi
    Citation: BMC Bioinformatics 2009 10:435
  33. Improvements in high-throughput technology and its increasing use have led to the generation of many highly complex datasets that often address similar biological questions. Combining information from these st...

    Authors: Clark D Jeffries, William O Ward, Diana O Perkins and Fred A Wright
    Citation: BMC Bioinformatics 2009 10:431
  34. Metagenomics is a new field of research on natural microbial communities. High-throughput sequencing techniques like 454 or Solexa-Illumina promise new possibilities as they are able to produce huge amounts of...

    Authors: Wolfgang Gerlach, Sebastian Jünemann, Felix Tille, Alexander Goesmann and Jens Stoye
    Citation: BMC Bioinformatics 2009 10:430
  35. Recently introduced pathway-based approach is promising and advantageous to improve the efficiency of analyzing genome-wide association scan (GWAS) data to identify disease variants by jointly considering vari...

    Authors: Yan-Fang Guo, Jian Li, Yuan Chen, Li-Shu Zhang and Hong-Wen Deng
    Citation: BMC Bioinformatics 2009 10:429

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