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sybil (version 1.0.1)

readTSVmod: Read a Metabolic Network in a TSV (CSV) Format

Description

The function readTSVmod reads metabolic networks in text files, following a character-separated value format. Each line should contain one entry; the default value separator is a tab. Output files from the BiGG database are compatible.

Usage

readTSVmod(prefix, suffix,
             reactList, metList = NA, modDesc = NA,
             fielddelim = "", entrydelim = ", ", extMetFlag = "b",
             excludeComments = TRUE,
             oneSubSystem = TRUE,
             mergeMet = TRUE,
             balanceReact = TRUE,
             remUnusedMetReact = TRUE,
             singletonMet = FALSE,
             deadEndMet = FALSE,
             remMet = FALSE,
             constrMet = FALSE,
             tol = SYBIL_SETTINGS("TOLERANCE"),
             verboseMode = 2,
             loglevel = -1,
             logfile = NA,
             logfileEnc = NA,
             fpath = SYBIL_SETTINGS("PATH_TO_MODEL"),
             def_bnd = SYBIL_SETTINGS("MAXIMUM"),
             quoteChar = "",
             commentChar, ...)
prefix{
    A single character string giving the prefix for three possible input files
    (see Details below).
  }
  suffix{
    A single character string giving the file name extension. If missing, the
    value of suffix depends on the argument fielddelim, see
    Details below.
Default: "tsv".
  }
  reactList{
    A single character vector giving a file name containing a reaction list.
    Only necessary, if argument suffix is empty.
  }
  metList{
    A single character vector giving a file name containing a metabolite
    list.
Default: NA.
  }
  modDesc{
    A single character vector giving a file name containing a model
    description.
Default: NA.
  }
  fielddelim{
    A single character string giving the value separator.
Default: "t".
  }
  entrydelim{
    A single character string giving the a separator for values containing
    more than one entry.
Default: ", ".
  }
  extMetFlag{
    A single character string giving the identificator for metabolites which
    are outside the system boundary. Only necessary, if the model is a closed
    one.
Default: "b".
  }
  excludeComments{
    A boolean value. Sometimes, the reaction abbreviations and/or the metabolite
    abbreviations contain comments in square brackets. If set to TRUE,
    these comments will be removed. If set to FALSE, whitespaces included
    in comments in metabolite abbreviations will be removed. Comments in
    reaction abbreviations stay unchanged.
Default: TRUE.
  }
  oneSubSystem{
    A boolean value. Ignore parameter entrydelim for the field
    subsystem, if every reaction belongs to exactly one sys system.
Default: TRUE.
  }
  mergeMet{
    Boolean: if set to TRUE, metabolites used more than once as reactand
    or product in a particular reaction are added up, see details below. If set
    to FALSE, the last value is used without warning.
Default: TRUE.
  }
  balanceReact{
    Boolean: if set to TRUE, metabolites used as reactand and product in
    a particular reaction at the same time are balanced, see details below. If
    set to FALSE the last value is used without warning (reactands before
    products).
Default: TRUE.
  }
  remUnusedMetReact{
    Boolean: if set to TRUE, metabolites and reactions which are not used in the
    stoichiometric matrix will be removed. A metabolite or a reaction is
    considered as unused, if the corresponding element  of rowSums
    (metabolites) or colSums (reactions) of the binary version of the
    stoichiometric matrix is zero, see details below. If set to FALSE,
    only a warning is given.
Default: FALSE.
  }
  singletonMet{
    Boolean: if set to TRUE, metabolites appearing only once in the
    stoichiometric matrix are identified. Metabolites appear only
    once, if rowSums of the binary stoichiometric matrix is one in
    the corresponding row, see details below.
Default: FALSE.
  }
  deadEndMet{
    Boolean: if set to TRUE, metabolites which are produced but not consumed, or
    vice versa are identified, see details below. If both arguments
    singletonMet and deadEndMet are set to TRUE, the
    function will first look for singleton metabolites, and exclude them (and
    the corresponding reactions) from the search list. Afterwards, dead end
    metabolites are searched only in the smaller model.
Default: FALSE.
  }
  remMet{
    Boolean: if set to TRUE, metabolites identified as singleton or dead end
    metabolites will be removed from the model. Additionally, reactions
    containing such metabolites will be removed also.
Default: FALSE.
  }
  constrMet{
    Boolean: if set to TRUE, reactions containing metabolites identified as
    singleton or dead end metabolites will be constrained to zero.
Default: FALSE.
  }
  tol{
    A single numeric value, giving the smallest positive floating point number
    unequal to zero, see details below.
Default: SYBIL_SETTINGS("TOLERANCE").
  }
  verboseMode{
    Single integer value, see sybilLog for possible values.
Default: 2.
  }
  loglevel{
    Single integer value, see sybilLog for possible values.
Default: -1.
  }
  logfile{
    A single character string giving the filename of the logfile.
    The value of logfile gets prefixed with fpath. If
    logfile is set to NA and loglevel is > -1,
    a default filename is used (see sybilLog for details).
Default: NA.
  }
  logfileEnc{
    A single character string giving the encoding for the logfile. If set to
    NA, the default encoding is used: getOption("encoding").
    If logfileEnc is set to something different, the option
    useFancyQuotes is turned
    off: options(useFancyQuotes = FALSE).
Default: NA.
  }
  fpath{
    A single character string giving the path to a certain directory containing
    the model files.
Default: SYBIL_SETTINGS("PATH_TO_MODEL").
  }
  def_bnd{
    A single numeric value. Absolute value for uppper and lower bounds for
    reaction bounds.
Default: SYBIL_SETTINGS("MAXIMUM").
  }
  quoteChar{
    Set of quoting characters used for the argument quote in
    read.table, see there for details.
Default: "" (disable quoting).
  }
  commentChar{
    A single character used for the argument comment.char in
    read.table, see there for details. If a comment char is
    needed, e.g. @ (at) seems to be a good one.
Default: "".
  }
  ...{
    Further arguments passed to read.table, e.g. argument
    quote, comment.char or argument fill, if some lines do
    not have enough elements. If all fields are in double quotes, for example,
    set quote to """.
  }
A metabolic model consists of three input files:
  
  1. _react.containing all reactions.
  2. _met.containing all metabolites.
  3. _desc.containing a model description.

  All of these files must be character separated value files (for a detailed
  format description and examples, see package vignette).  The argument
  prefix is the part of the filenames, all three have in common (e.g. if
  they where produced by modelorg2tsv).
  Alternativly, the arguments reactList, metList and
  modDesc can be used.  A file containing all reactions must be there,
  everything else is optional.
  If suffix is missing, it is set according to the value of
  fielddelim:
  ll{
      "t"   	"tsv" 
";"    	"csv" 
","    	"csv" 
"|"    	"dsv" 
anything else 	"dsv" 
}
  The argument ... is passed to read.table.  It could be
  necessary, to turn off quoting quote = "", if e.g. metabolite names
  contain quoting characters "'" like in
  3',5'-bisphosphate nucleotidase.
  The input files are read using the function read.table.  The
  argument header is set to TRUE and the argument sep is
  set to the value of fielddelim.  Everything else can be passed via
  the ... argument.
  The header for the reactions list may have the following columns:
  ll{
      "abbreviation" 	a unique reaction id                       
"name"         	a reaction name                            
"equation"     	the reaction equation                      
"reversible"   	TRUE, if the reaction is reversible        
"compartment"  	reaction compartment(s) (currently unused) 
"lowbnd"       	lower bound                                
"uppbnd"       	upper bound                                
"obj_coef"     	objective coeficient                       
"rule"         	gene to reaction association               
"subsystem"    	subsystem of the reaction                  
}
  Every entry except for "equation" is optional.
  The header for the metabolites list may have the following columns:
  ll{
      "abbreviation" 	a unique metabolite id                    
"name"         	a metabolite name                         
"compartment"  	metabolite compartment (currently unused) 
}
  If a metabolite list is provided, it is supposed to contain at least the
  entries "abbreviation" and "name".
  The header for the model description file may have the following columns:
  ll{
      "name"         	a name for the model             
"id"           	a shorter model id               
"description"  	a model description              
"compartment"  	the compartments                 
"abbreviation" 	unique compartment abbreviations 
"Nmetabolites" 	number of metabolites            
"Nreactions"   	number of reactions              
"Ngenes"       	number of independend genes      
"Nnnz"         	number of non-zero elements in
                                 the stoichiometric matrix        
}
  If a model description file is provided, it is supposed to contain at least
  the entries "name" and "id".  Otherwise, the filename of the
  reactions list will be used.
  The compartments in which a reaction takes place is determined by the
  compartment flags of the participating metabolites.
  All fields in the output files of modelorg2tsv are in double
  quotes. In order to read them, set argument quote to """.
  Please read the package vignette for detailed information about input formats
  and examples.
  If a metabolite is used more than once as product or
  reactand of a particular reaction, it is merged:
  a + (2) a is converted to (3) a
  and a warning will be given.
  If a metabolite is used first as reactand and then as
  product of a particular reaction, the reaction is
  balanced:
      (2) b + a -> b + c
  is converted to
      b + a ->     c
  A binary version of the stoichiometric matrix $S$ is constructed
  via $\left|S\right| > tol$.
  A binary version of the stoichiometric matrix $S$ is scanned for reactions
  and metabolites which are not used in S. If there are some, a warning will be
  given and the corresponding reactions and metabolites will be removed from
  the model if remUnusedMetReact is set to TRUE.
  The binary version of the stoichiometric matrix $S$ is scanned for
  metabolites, which are used only once in S. If there are some, at least
  warning will be given. If either constrMet or remMet is set to
  TRUE, the binary version of $S$ is scanned for paths of singleton
  metabolites. If constrMet is set to TRUE, reactions containing
  those metabolites will be constrained to zero; if remMet is set to
  TRUE, the metabolites and the reactions containing those metabolites
  will be removed from the network.
  In order to find path of singleton metabolites a binary version of the
  stiochiometric matrix $S$ is used. Sums of rows gives the vektor of
  metabolite usage, each element is the number of reactions a metabolite
  parcipitates.  A single metabolite (singleton) is a metabolite with a row sum
  of zero. All columns in $S$ (reactions) containing singleton metabolites
  will be set to zero. And again, singleton metabolites will be searched until
  none are found.
  The algorithm to find dead end metabolites works in a quite similar way, but
  not in the binary version of the stroichiometric matrix. Here, metabolite
  i is considered as dead end, if it is for example produced by reaction
  j but not used by any other reaction k.
An instance of class modelorg.
The BiGG database http://bigg.ucsd.edu/.
  Schellenberger, J., Park, J. O., Conrad, T. C., and Palsson, B. Ø., (2010)
  BiGG: a Biochemical Genetic and Genomic knowledgebase of large scale metabolic
  reconstructions. BMC Bioinformatics 11, 213.
  Becker, S. A., Feist, A. M., Mo, M. L., Hannum, G., Palsson, B. Ø.  and
  Herrgard, M. J. (2007) Quantitative prediction of cellular metabolism with
  constraint-based models: the COBRA Toolbox. Nat Protoc 2,
  727--738.
  Schellenberger, J., Que, R., Fleming, R. M. T., Thiele, I., Orth, J. D.,
  Feist, A. M., Zielinski, D. C., Bordbar, A., Lewis, N. E., Rahmanian, S.,
  Kang, J., Hyduke, D. R. and Palsson, B. Ø. (2011) Quantitative prediction of
  cellular metabolism with constraint-based models: the COBRA Toolbox v2.0.
  Nat Protoc 6, 1290--1307.
[object Object]
read.table, modelorg2tsv,
  modelorg, sybilLog.
file

Arguments

encoding

utf8