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Update example parameter files
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docs/ParameterFiles/MSGFPlus_PartTryp_DynMetOx_ProOx_Stat_CysAlk_TMT_6Plex_20ppmParTol.txt

+31-24
Original file line numberDiff line numberDiff line change
@@ -1,86 +1,93 @@
1-
#Parent mass tolerance
1+
# Parent mass tolerance
22
# Examples: 2.5Da or 30ppm
33
# Use comma to set asymmetric values, for example "0.5Da,2.5Da" will set 0.5Da to the left (expMass<theoMass) and 2.5Da to the right (expMass>theoMass)
44
PrecursorMassTolerance=20ppm
55

6-
#Max Number of Modifications per peptide
6+
# Max Number of Modifications per peptide
77
# If this value is large, the search will be slow
88
NumMods=3
99

10-
#Modifications (see below for examples)
10+
# Modifications (see below for examples)
1111
StaticMod=229.1629, *, fix, N-term, TMT6plex
1212
StaticMod=229.1629, K, fix, any, TMT6plex
1313
StaticMod=C2H3N1O1, C, fix, any, Carbamidomethyl # Fixed Carbamidomethyl C (alkylation, +57.0215)
1414

1515
DynamicMod=O1, MP, opt, any, Oxidation # Oxidized methionine and proline
1616

17-
#Fragmentation Method
17+
# Fragmentation Method
1818
# 0 means as written in the spectrum or CID if no info (Default)
1919
# 1 means CID
2020
# 2 means ETD
2121
# 3 means HCD
2222
# 4 means Merge spectra from the same precursor (e.g. CID/ETD pairs, CID/HCD/ETD triplets)
2323
FragmentationMethodID=0
2424

25-
#Instrument ID
25+
# Instrument ID
2626
# 0 means Low-res LCQ/LTQ (Default for CID and ETD); use InstrumentID=0 if analyzing a dataset with low-res CID and high-res HCD spectra
2727
# 1 means High-res LTQ (Default for HCD; also appropriate for high res CID); use InstrumentID=1 for Orbitrap, Lumos, and QEHFX instruments
2828
# 2 means TOF
2929
# 3 means Q-Exactive
3030
InstrumentID=1
3131

32-
#Enzyme ID
33-
# 0 means No enzyme used
34-
# 1 means Trypsin (Default); use this along with NTT=0 for a no-enzyme search of a tryptically digested sample
35-
# 2: Chymotrypsin, 3: Lys-C, 4: Lys-N, 5: Glu-C, 6: Arg-C, 7: Asp-N, 8: alphaLP, 9: No Enzyme (for peptidomics)
32+
# Enzyme ID
33+
# 0 means unspecific cleavage (cleave after any residue)
34+
# 1 means Trypsin (Default); optionally use this along with NTT=0 for a no-enzyme-specificity search of a tryptically digested sample
35+
# 2: Chymotrypsin, 3: Lys-C, 4: Lys-N, 5: Glu-C, 6: Arg-C, 7: Asp-N, 8: alphaLP, 9: No Cleavage (for peptidomics)
3636
EnzymeID=1
3737

38-
#Isotope error range
38+
# Isotope error range
3939
# Takes into account of the error introduced by choosing non-monoisotopic peak for fragmentation.
4040
# Useful for accurate precursor ion masses
4141
# Ignored if the parent mass tolerance is > 0.5Da or 500ppm
4242
# The combination of -t and -ti determins the precursor mass tolerance.
4343
# e.g. "-t 20ppm -ti -1,2" tests abs(exp-calc-n*1.00335Da)<20ppm for n=-1, 0, 1, 2.
4444
IsotopeErrorRange=-1,1
4545

46-
#Number of tolerable termini
46+
# Number of tolerable termini
4747
# The number of peptide termini that must have been cleaved by the enzyme (default 1)
4848
# For trypsin, 2 means fully tryptic only, 1 means partially tryptic, and 0 means no-enzyme search
4949
NTT=1
5050

51-
#Target/Decoy search mode
51+
# Control N-terminal methionine cleavage
52+
# 0 means to consider protein N-term Met cleavage (Default)
53+
# 1 means to ignore protein N-term Met cleavage
54+
IgnoreMetCleavage=0
55+
56+
# Target/Decoy search mode
5257
# 0 means don't search decoy database (default)
5358
# 1 means search decoy database to compute FDR (source FASTA file must be forward-only proteins)
5459
TDA=1
5560

56-
#Number of Threads (by default, uses all available cores)
61+
# Number of Threads (by default, uses all available cores)
5762
NumThreads=All
5863

59-
#Minimum peptide length to consider
64+
# Minimum peptide length to consider
6065
MinPepLength=6
6166

62-
#Maximum peptide length to consider
67+
# Maximum peptide length to consider
6368
MaxPepLength=50
6469

65-
#Minimum precursor charge to consider (if not specified in the spectrum)
70+
# Minimum precursor charge to consider (if not specified in the spectrum)
6671
MinCharge=2
6772

68-
#Maximum precursor charge to consider (if not specified in the spectrum)
73+
# Maximum precursor charge to consider (if not specified in the spectrum)
6974
MaxCharge=5
7075

71-
#Number of matches per spectrum to be reported
72-
#If this value is greater than 1 then the FDR values computed by MS-GF+ will be skewed by high-scoring 2nd and 3rd hits
76+
# Number of matches per spectrum to be reported
77+
# If this value is greater than 1, the FDR values computed by MS-GF+ will be skewed by high-scoring 2nd and 3rd hits
7378
NumMatchesPerSpec=1
7479

75-
#Amino Acid Modification Examples
76-
# Specific static modifications using one or more StaticMod= entries
77-
# Specific dynamic modifications using one or more DynamicMod= entries
80+
# Amino Acid Modification Examples
81+
# Specify static modifications using one or more StaticMod= entries
82+
# Specify dynamic modifications using one or more DynamicMod= entries
7883
# Modification format is:
79-
# Mass or CompositionStr, Residues, ModType, Position, Name (all the five fields are required).
84+
# Mass or CompositionString, Residues, ModType, Position, Name (all five fields are required).
85+
# CompositionString can only contain a limited set of elements, primarily C H N O S or P
86+
#
8087
# Examples:
8188
# C2H3N1O1, C, fix, any, Carbamidomethyl # Fixed Carbamidomethyl C (alkylation)
8289
# O1, M, opt, any, Oxidation # Oxidation M
83-
# 15.994915, M, opt, any, Oxidation # Oxidation M (mass is used instead of CompositionStr)
90+
# 15.994915, M, opt, any, Oxidation # Oxidation M (mass is used instead of CompositionString)
8491
# H-1N-1O1, NQ, opt, any, Deamidated # Negative numbers are allowed.
8592
# CH2, K, opt, any, Methyl # Methylation K
8693
# C2H2O1, K, opt, any, Acetyl # Acetylation K

docs/ParameterFiles/MSGFPlus_PartTryp_DynMetOx_Stat_CysAlk_TMT_6Plex_20ppmParTol.txt

+27-22
Original file line numberDiff line numberDiff line change
@@ -1,88 +1,93 @@
1-
#Parent mass tolerance
1+
# Parent mass tolerance
22
# Examples: 2.5Da or 30ppm
33
# Use comma to set asymmetric values, for example "0.5Da,2.5Da" will set 0.5Da to the left (expMass<theoMass) and 2.5Da to the right (expMass>theoMass)
44
PrecursorMassTolerance=20ppm
55

6-
#Max Number of Modifications per peptide
6+
# Max Number of Modifications per peptide
77
# If this value is large, the search will be slow
88
NumMods=3
99

10-
#Modifications (see below for examples)
10+
# Modifications (see below for examples)
1111
StaticMod=229.1629, *, fix, N-term, TMT6plex
1212
StaticMod=229.1629, K, fix, any, TMT6plex
1313
StaticMod=C2H3N1O1, C, fix, any, Carbamidomethyl # Fixed Carbamidomethyl C (alkylation, +57.0215)
1414

1515
DynamicMod=O1, M, opt, any, Oxidation # Oxidized methionine
1616

17-
#Fragmentation Method
17+
# Fragmentation Method
1818
# 0 means as written in the spectrum or CID if no info (Default)
1919
# 1 means CID
2020
# 2 means ETD
2121
# 3 means HCD
2222
# 4 means Merge spectra from the same precursor (e.g. CID/ETD pairs, CID/HCD/ETD triplets)
2323
FragmentationMethodID=0
2424

25-
#Instrument ID
25+
# Instrument ID
2626
# 0 means Low-res LCQ/LTQ (Default for CID and ETD); use InstrumentID=0 if analyzing a dataset with low-res CID and high-res HCD spectra
2727
# 1 means High-res LTQ (Default for HCD; also appropriate for high res CID); use InstrumentID=1 for Orbitrap, Lumos, and QEHFX instruments
2828
# 2 means TOF
2929
# 3 means Q-Exactive
3030
InstrumentID=1
3131

32-
#Enzyme ID
33-
# 0 means No enzyme used
34-
# 1 means Trypsin (Default); use this along with NTT=0 for a no-enzyme search of a tryptically digested sample
35-
# 2: Chymotrypsin, 3: Lys-C, 4: Lys-N, 5: Glu-C, 6: Arg-C, 7: Asp-N, 8: alphaLP, 9: No Enzyme (for peptidomics)
32+
# Enzyme ID
33+
# 0 means unspecific cleavage (cleave after any residue)
34+
# 1 means Trypsin (Default); optionally use this along with NTT=0 for a no-enzyme-specificity search of a tryptically digested sample
35+
# 2: Chymotrypsin, 3: Lys-C, 4: Lys-N, 5: Glu-C, 6: Arg-C, 7: Asp-N, 8: alphaLP, 9: No Cleavage (for peptidomics)
3636
EnzymeID=1
3737

38-
#Isotope error range
38+
# Isotope error range
3939
# Takes into account of the error introduced by choosing non-monoisotopic peak for fragmentation.
4040
# Useful for accurate precursor ion masses
4141
# Ignored if the parent mass tolerance is > 0.5Da or 500ppm
4242
# The combination of -t and -ti determins the precursor mass tolerance.
4343
# e.g. "-t 20ppm -ti -1,2" tests abs(exp-calc-n*1.00335Da)<20ppm for n=-1, 0, 1, 2.
4444
IsotopeErrorRange=-1,2
4545

46-
#Number of tolerable termini
46+
# Number of tolerable termini
4747
# The number of peptide termini that must have been cleaved by the enzyme (default 1)
4848
# For trypsin, 2 means fully tryptic only, 1 means partially tryptic, and 0 means no-enzyme search
4949
NTT=1
5050

51-
#Target/Decoy search mode
51+
# Control N-terminal methionine cleavage
52+
# 0 means to consider protein N-term Met cleavage (Default)
53+
# 1 means to ignore protein N-term Met cleavage
54+
IgnoreMetCleavage=0
55+
56+
# Target/Decoy search mode
5257
# 0 means don't search decoy database (default)
5358
# 1 means search decoy database to compute FDR (source FASTA file must be forward-only proteins)
5459
TDA=1
5560

56-
#Number of Threads (by default, uses all available cores)
61+
# Number of Threads (by default, uses all available cores)
5762
NumThreads=All
5863

59-
#Minimum peptide length to consider
64+
# Minimum peptide length to consider
6065
MinPepLength=6
6166

62-
#Maximum peptide length to consider
67+
# Maximum peptide length to consider
6368
MaxPepLength=50
6469

65-
#Minimum precursor charge to consider (if not specified in the spectrum)
70+
# Minimum precursor charge to consider (if not specified in the spectrum)
6671
MinCharge=2
6772

68-
#Maximum precursor charge to consider (if not specified in the spectrum)
73+
# Maximum precursor charge to consider (if not specified in the spectrum)
6974
MaxCharge=5
7075

71-
#Number of matches per spectrum to be reported
72-
#If this value is greater than 1 then the FDR values computed by MS-GF+ will be skewed by high-scoring 2nd and 3rd hits
76+
# Number of matches per spectrum to be reported
77+
# If this value is greater than 1, the FDR values computed by MS-GF+ will be skewed by high-scoring 2nd and 3rd hits
7378
NumMatchesPerSpec=1
7479

75-
#Amino Acid Modification Examples
80+
# Amino Acid Modification Examples
7681
# Specify static modifications using one or more StaticMod= entries
7782
# Specify dynamic modifications using one or more DynamicMod= entries
7883
# Modification format is:
79-
# Mass or CompositionString, Residues, ModType, Position, Name (all the five fields are required).
84+
# Mass or CompositionString, Residues, ModType, Position, Name (all five fields are required).
8085
# CompositionString can only contain a limited set of elements, primarily C H N O S or P
8186
#
8287
# Examples:
8388
# C2H3N1O1, C, fix, any, Carbamidomethyl # Fixed Carbamidomethyl C (alkylation)
8489
# O1, M, opt, any, Oxidation # Oxidation M
85-
# 15.994915, M, opt, any, Oxidation # Oxidation M (mass is used instead of CompositionStr)
90+
# 15.994915, M, opt, any, Oxidation # Oxidation M (mass is used instead of CompositionString)
8691
# H-1N-1O1, NQ, opt, any, Deamidated # Negative numbers are allowed.
8792
# CH2, K, opt, any, Methyl # Methylation K
8893
# C2H2O1, K, opt, any, Acetyl # Acetylation K

docs/ParameterFiles/MSGFPlus_PartTryp_DynMetOx_Stat_CysAlk_iTRAQ_8Plex_20ppmParTol.txt

+31-24
Original file line numberDiff line numberDiff line change
@@ -1,86 +1,93 @@
1-
#Parent mass tolerance
1+
# Parent mass tolerance
22
# Examples: 2.5Da or 30ppm
33
# Use comma to set asymmetric values, for example "0.5Da,2.5Da" will set 0.5Da to the left (expMass<theoMass) and 2.5Da to the right (expMass>theoMass)
44
PrecursorMassTolerance=20ppm
55

6-
#Max Number of Modifications per peptide
6+
# Max Number of Modifications per peptide
77
# If this value is large, the search will be slow
88
NumMods=3
99

10-
#Modifications (see below for examples)
10+
# Modifications (see below for examples)
1111
StaticMod=304.205353, *, fix, N-term, iTRAQ8plex
1212
StaticMod=304.205353, K, fix, any, iTRAQ8plex
1313
StaticMod=C2H3N1O1, C, fix, any, Carbamidomethyl # Fixed Carbamidomethyl C (alkylation, +57.0215)
1414

1515
DynamicMod=O1, M, opt, any, Oxidation # Oxidized methionine
1616

17-
#Fragmentation Method
17+
# Fragmentation Method
1818
# 0 means as written in the spectrum or CID if no info (Default)
1919
# 1 means CID
2020
# 2 means ETD
2121
# 3 means HCD
2222
# 4 means Merge spectra from the same precursor (e.g. CID/ETD pairs, CID/HCD/ETD triplets)
2323
FragmentationMethodID=0
2424

25-
#Instrument ID
25+
# Instrument ID
2626
# 0 means Low-res LCQ/LTQ (Default for CID and ETD); use InstrumentID=0 if analyzing a dataset with low-res CID and high-res HCD spectra
2727
# 1 means High-res LTQ (Default for HCD; also appropriate for high res CID); use InstrumentID=1 for Orbitrap, Lumos, and QEHFX instruments
2828
# 2 means TOF
2929
# 3 means Q-Exactive
3030
InstrumentID=1
3131

32-
#Enzyme ID
33-
# 0 means No enzyme used
34-
# 1 means Trypsin (Default); use this along with NTT=0 for a no-enzyme search of a tryptically digested sample
35-
# 2: Chymotrypsin, 3: Lys-C, 4: Lys-N, 5: Glu-C, 6: Arg-C, 7: Asp-N, 8: alphaLP, 9: No Enzyme (for peptidomics)
32+
# Enzyme ID
33+
# 0 means unspecific cleavage (cleave after any residue)
34+
# 1 means Trypsin (Default); optionally use this along with NTT=0 for a no-enzyme-specificity search of a tryptically digested sample
35+
# 2: Chymotrypsin, 3: Lys-C, 4: Lys-N, 5: Glu-C, 6: Arg-C, 7: Asp-N, 8: alphaLP, 9: No Cleavage (for peptidomics)
3636
EnzymeID=1
3737

38-
#Isotope error range
38+
# Isotope error range
3939
# Takes into account of the error introduced by choosing non-monoisotopic peak for fragmentation.
4040
# Useful for accurate precursor ion masses
4141
# Ignored if the parent mass tolerance is > 0.5Da or 500ppm
4242
# The combination of -t and -ti determins the precursor mass tolerance.
4343
# e.g. "-t 20ppm -ti -1,2" tests abs(exp-calc-n*1.00335Da)<20ppm for n=-1, 0, 1, 2.
4444
IsotopeErrorRange=-1,1
4545

46-
#Number of tolerable termini
46+
# Number of tolerable termini
4747
# The number of peptide termini that must have been cleaved by the enzyme (default 1)
4848
# For trypsin, 2 means fully tryptic only, 1 means partially tryptic, and 0 means no-enzyme search
4949
NTT=1
5050

51-
#Target/Decoy search mode
51+
# Control N-terminal methionine cleavage
52+
# 0 means to consider protein N-term Met cleavage (Default)
53+
# 1 means to ignore protein N-term Met cleavage
54+
IgnoreMetCleavage=0
55+
56+
# Target/Decoy search mode
5257
# 0 means don't search decoy database (default)
5358
# 1 means search decoy database to compute FDR (source FASTA file must be forward-only proteins)
5459
TDA=1
5560

56-
#Number of Threads (by default, uses all available cores)
61+
# Number of Threads (by default, uses all available cores)
5762
NumThreads=All
5863

59-
#Minimum peptide length to consider
64+
# Minimum peptide length to consider
6065
MinPepLength=6
6166

62-
#Maximum peptide length to consider
67+
# Maximum peptide length to consider
6368
MaxPepLength=50
6469

65-
#Minimum precursor charge to consider (if not specified in the spectrum)
70+
# Minimum precursor charge to consider (if not specified in the spectrum)
6671
MinCharge=2
6772

68-
#Maximum precursor charge to consider (if not specified in the spectrum)
73+
# Maximum precursor charge to consider (if not specified in the spectrum)
6974
MaxCharge=5
7075

71-
#Number of matches per spectrum to be reported
72-
#If this value is greater than 1 then the FDR values computed by MS-GF+ will be skewed by high-scoring 2nd and 3rd hits
76+
# Number of matches per spectrum to be reported
77+
# If this value is greater than 1, the FDR values computed by MS-GF+ will be skewed by high-scoring 2nd and 3rd hits
7378
NumMatchesPerSpec=1
7479

75-
#Amino Acid Modification Examples
76-
# Specific static modifications using one or more StaticMod= entries
77-
# Specific dynamic modifications using one or more DynamicMod= entries
80+
# Amino Acid Modification Examples
81+
# Specify static modifications using one or more StaticMod= entries
82+
# Specify dynamic modifications using one or more DynamicMod= entries
7883
# Modification format is:
79-
# Mass or CompositionStr, Residues, ModType, Position, Name (all the five fields are required).
84+
# Mass or CompositionString, Residues, ModType, Position, Name (all five fields are required).
85+
# CompositionString can only contain a limited set of elements, primarily C H N O S or P
86+
#
8087
# Examples:
8188
# C2H3N1O1, C, fix, any, Carbamidomethyl # Fixed Carbamidomethyl C (alkylation)
8289
# O1, M, opt, any, Oxidation # Oxidation M
83-
# 15.994915, M, opt, any, Oxidation # Oxidation M (mass is used instead of CompositionStr)
90+
# 15.994915, M, opt, any, Oxidation # Oxidation M (mass is used instead of CompositionString)
8491
# H-1N-1O1, NQ, opt, any, Deamidated # Negative numbers are allowed.
8592
# CH2, K, opt, any, Methyl # Methylation K
8693
# C2H2O1, K, opt, any, Acetyl # Acetylation K

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