• DocumentCode
    902048
  • Title

    Peptide Mass Fingerprinting Using Field-Programmable Gate Arrays

  • Author

    Bogdan, I.A. ; Coca, D. ; Beynon, R.J.

  • Author_Institution
    Autom. Control & Syst. Eng. Dept., Sheffield Universityd Univ., Sheffield
  • Volume
    3
  • Issue
    3
  • fYear
    2009
  • fDate
    6/1/2009 12:00:00 AM
  • Firstpage
    142
  • Lastpage
    149
  • Abstract
    The reconfigurable computing paradigm, which exploits the flexibility and versatility of field-programmable gate arrays (FPGAs), has emerged as a powerful solution for speeding up time-critical algorithms. This paper describes a reconfigurable computing solution for processing raw mass spectrometric data generated by MALDI-TOF instruments. The hardware-implemented algorithms for denoising, baseline correction, peak identification, and deisotoping, running on a Xilinx Virtex-2 FPGA at 180 MHz, generate a mass fingerprint that is over 100 times faster than an equivalent algorithm written in C, running on a Dual 3-GHz Xeon server. The results obtained using the FPGA implementation are virtually identical to those generated by a commercial software package MassLynx.
  • Keywords
    biology computing; field programmable gate arrays; mass spectroscopy; proteins; proteomics; FPGA; MALDI-TOF; MassLynx; Xilinx Virtex-2; baseline correction; denoising; field-programmable gate arrays; frequency 180 MHz; peak identification; peptide mass fingerprinting; Concurrent computing; Databases; Field programmable gate arrays; Fingerprint recognition; Hardware; Mass spectroscopy; Microprocessors; Peptides; Proteins; Proteomics; Biomedical computing; field-programmable gate arrays (FPGAs); mass spectrometry; optimization methods; proteins;
  • fLanguage
    English
  • Journal_Title
    Biomedical Circuits and Systems, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    1932-4545
  • Type

    jour

  • DOI
    10.1109/TBCAS.2008.2010945
  • Filename
    4956975