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Mustafa Tekpinar
PRESCOTT
Commits
33693642
Commit
33693642
authored
May 30, 2022
by
Mustafa Tekpinar
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Some minor code annotations!
parent
1383201b
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3 changed files
with
18 additions
and
8 deletions
+18
-8
computePred.R
computePred.R
+1
-1
gemmeAnal.py
gemmeAnal.py
+12
-7
pred.R
pred.R
+5
-0
No files found.
computePred.R
View file @
33693642
...
...
@@ -181,7 +181,7 @@ if((normWeightMode=="max-trace-pc") | (normWeightMode=="max-pc-trace")){
}
}
else
{
print
(
"ERROR: Unknown --normWeightMode selected!"
)
print
(
"It can only be 'trace', 'pc', 'cv', 'max-trace-pc', 'max-trace-cv', 'max-trace-pc-cv' or 'half-cv+pc'!"
)
print
(
"It can only be 'trace', 'pc', 'cv', '
dfi', '
max-trace-pc', 'max-trace-cv', 'max-trace-pc-cv' or 'half-cv+pc'!"
)
}
print
(
trace
)
...
...
gemmeAnal.py
View file @
33693642
...
...
@@ -13,8 +13,11 @@ import subprocess
import
shutil
# Extract the query sequence from the input alignment
def
extractQuerySeq
(
filename
):
"""
# Extract the query sequence from the input alignment
"""
fIN
=
open
(
filename
,
"r"
)
lines
=
fIN
.
readlines
()
...
...
@@ -35,21 +38,21 @@ def extractQuerySeq(filename):
fOUT
.
close
()
return
prot
,
seq
,
i
-
1
# Get the number of sequences in a multi-fasta file
def
getNbSeq
(
filename
):
def
getNbSeq
(
filename
):
"""
# Get the number of sequences in a multi-fasta file
"""
if
filename
!=
''
:
proc
=
subprocess
.
Popen
(
"grep -c '^>' "
+
filename
,
stdout
=
subprocess
.
PIPE
,
shell
=
True
)
return
int
(
proc
.
stdout
.
read
())
else
:
return
0
# Create a PDB file with dummy CA atoms based on the query sequence
def
createPDB
(
prot
,
seq
):
"""
If there is not a real PDB file for a given sequence,
create a fake PDB containing only CA atoms.
create a fake PDB containing only
dummy
CA atoms.
"""
d
=
{
'C'
:
'CYS'
,
'D'
:
'ASP'
,
'S'
:
'SER'
,
'Q'
:
'GLN'
,
'K'
:
'LYS'
,
'I'
:
'ILE'
,
'P'
:
'PRO'
,
'T'
:
'THR'
,
'F'
:
'PHE'
,
'N'
:
'ASN'
,
...
...
@@ -63,8 +66,10 @@ def createPDB(prot,seq):
i
+=
1
fOUT
.
close
()
# Edit JET configuration file with correct number of Seqs & MSA
def
editConfJET
(
N
):
"""
# Edit JET configuration file with correct number of Seqs & MSA
"""
reCode
=
subprocess
.
call
(
"sed -i 's/results
\t\t
5000/results
\t\t
"
+
str
(
N
)
+
"/' default.conf"
,
shell
=
True
)
return
(
reCode
)
...
...
pred.R
View file @
33693642
...
...
@@ -224,6 +224,7 @@ which.class<-function(a,alphabet){
# log-odd ratio between the mutated and wild-type sequence counts
computePredNbSeqs
<-
function
(
wt
,
nbseqs
){
#Equation 7 in https://doi.org/10.1093/molbev/msz179
n
=
length
(
wt
)
pred
=
matrix
(
nc
=
n
,
nr
=
20
)
rownames
(
pred
)
=
aa
...
...
@@ -385,6 +386,8 @@ normalizePred<-function(pred, trace, wt){
return
(
-
normPred
)
}
# Equation 2 in https://doi.org/10.1093/molbev/msz179
normalizePredWithNbSeqsPC
<-
function
(
pred
,
trace
,
wt
,
alpha
,
nbSeqs
,
alphabet
){
n
=
length
(
trace
)
normPred
=
matrix
(
nc
=
n
,
nr
=
20
)
...
...
@@ -399,6 +402,8 @@ normalizePredWithNbSeqsPC<-function(pred, trace, wt, alpha, nbSeqs, alphabet){
for
(
a
in
aa
){
A
=
which.class
(
wt
[
i
],
alphabet
)
B
=
which.class
(
a
,
alphabet
)
# I think this is the place I should modify. alpha will become alpha[i]
normPred
[
a
,
i
]
=
alpha
*
normPred
[
a
,
i
]
-
(
1
-
alpha
)
*
log
(
max
(
1
,
nbseqs
[
B
,
i
])
/
nbseqs
[
A
,
i
])
}
normPred
[,
i
]
=
normPred
[,
i
]
*
trace
[
i
]
...
...
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