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DIADE
dynadiv
GrAnnoT
Commits
352a4b24
Commit
352a4b24
authored
1 year ago
by
nina.marthe_ird.fr
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corrigé la gestion des position des variations
parent
266289f3
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inference.py
+11
-12
11 additions, 12 deletions
inference.py
with
11 additions
and
12 deletions
inference.py
+
11
−
12
View file @
352a4b24
from
Graph_gff
import
Features
,
load_intersect
from
Graph_gff
import
Features
,
load_intersect
from
Functions
import
get_segment_sequence
,
convert_strand
from
Functions
import
get_segment_sequence
,
convert_strand
target_genome_name
=
"
genome
2
_chr10
"
target_genome_name
=
"
genome
5
_chr10
"
intersect_path
=
'
intersect.bed
'
intersect_path
=
'
intersect.bed
'
load_intersect
(
intersect_path
)
load_intersect
(
intersect_path
)
pos_seg
=
"
genome
2
_chr10.bed
"
pos_seg
=
"
genome
5
_chr10.bed
"
var
=
open
(
"
genome
2
_chr10_variations.txt
"
,
'
r
'
)
var
=
open
(
"
genome
5
_chr10_variations.txt
"
,
'
r
'
)
gfa
=
"
graph.gfa
"
gfa
=
"
graph.gfa
"
def
get_segments_sequence_and_paths
(
gfa
):
def
get_segments_sequence_and_paths
(
gfa
):
...
@@ -305,7 +305,7 @@ for cds_id in cds_var.keys():
...
@@ -305,7 +305,7 @@ for cds_id in cds_var.keys():
if
abs
(
length_alt
-
length_ref
)
%
3
==
0
:
# taille diff 3k -> pas de frame shift.
if
abs
(
length_alt
-
length_ref
)
%
3
==
0
:
# taille diff 3k -> pas de frame shift.
if
(
posVar
[
1
])
%
3
==
0
:
# taille diff 3k, position 3k
if
(
posVar
[
0
])
%
3
==
0
:
# taille diff 3k, position 3k
print
(
"
variation entre deux codons sans décalage du cadre de lecture
"
)
print
(
"
variation entre deux codons sans décalage du cadre de lecture
"
)
if
type_var
==
"
insertion
"
:
if
type_var
==
"
insertion
"
:
print
(
type_var
,
"
de
"
,
var
[
10
])
print
(
type_var
,
"
de
"
,
var
[
10
])
...
@@ -316,8 +316,8 @@ for cds_id in cds_var.keys():
...
@@ -316,8 +316,8 @@ for cds_id in cds_var.keys():
len_fragment_after
=
(
3
-
length_ref
)
%
3
len_fragment_after
=
(
3
-
length_ref
)
%
3
deleted_aa
=
traduction
(
get_rna
(
cds
.
sequence
[
posVar
[
1
]:
posVar
[
1
]
+
length_ref
+
len_fragment_after
]))
deleted_aa
=
traduction
(
get_rna
(
cds
.
sequence
[
posVar
[
0
]:
posVar
[
0
]
+
length_ref
+
len_fragment_after
]))
inserted_aa
=
traduction
(
get_rna
(
sequence_target
[
posVar
[
2
]:
posVar
[
2
]
+
length_alt
+
len_fragment_after
]))
inserted_aa
=
traduction
(
get_rna
(
sequence_target
[
posVar
[
1
]:
posVar
[
1
]
+
length_alt
+
len_fragment_after
]))
if
(
length_ref
!=
0
)
&
(
length_alt
!=
0
):
if
(
length_ref
!=
0
)
&
(
length_alt
!=
0
):
if
deleted_aa
!=
inserted_aa
:
if
deleted_aa
!=
inserted_aa
:
...
@@ -339,11 +339,11 @@ for cds_id in cds_var.keys():
...
@@ -339,11 +339,11 @@ for cds_id in cds_var.keys():
else
:
else
:
print
(
type_var
,
"
de
"
,
var
[
9
],
"
par
"
,
var
[
10
])
print
(
type_var
,
"
de
"
,
var
[
9
],
"
par
"
,
var
[
10
])
len_fragment_before
=
(
posVar
[
1
])
%
3
len_fragment_before
=
(
posVar
[
0
])
%
3
len_fragment_after
=
(
3
-
(
len_fragment_before
+
length_ref
))
%
3
len_fragment_after
=
(
3
-
(
len_fragment_before
+
length_ref
))
%
3
total_ins
=
sequence_target
[
posVar
[
2
]
-
len_fragment_before
:
posVar
[
2
]
+
length_alt
+
len_fragment_after
]
total_ins
=
sequence_target
[
posVar
[
1
]
-
len_fragment_before
:
posVar
[
1
]
+
length_alt
+
len_fragment_after
]
total_del
=
cds
.
sequence
[
posVar
[
1
]
-
len_fragment_before
:
posVar
[
1
]
+
length_ref
+
len_fragment_after
]
total_del
=
cds
.
sequence
[
posVar
[
0
]
-
len_fragment_before
:
posVar
[
0
]
+
length_ref
+
len_fragment_after
]
deleted_aa
=
traduction
(
get_rna
(
total_del
))
deleted_aa
=
traduction
(
get_rna
(
total_del
))
inserted_aa
=
traduction
(
get_rna
(
total_ins
))
inserted_aa
=
traduction
(
get_rna
(
total_ins
))
...
@@ -379,11 +379,10 @@ for cds_id in cds_var.keys():
...
@@ -379,11 +379,10 @@ for cds_id in cds_var.keys():
print
(
frame_shift
)
print
(
frame_shift
)
if
posVar
[
0
]
<=
3
:
# pour l'instant on cherche pas d'autre start.
if
posVar
[
1
]
<
3
:
# pour l'instant on cherche pas d'autre start.
print
(
"
codon start touché donc gène non fonctionnel
"
)
print
(
"
codon start touché donc gène non fonctionnel
"
)
#findOtherStart(cds,segments_on_target_genome)
#findOtherStart(cds,segments_on_target_genome)
break
#
break
...
...
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