Mirri 5.1.2

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2023-06-10 14:49:33 +01:00
parent e2278fd509
commit 322ed203d8
102 changed files with 1978 additions and 3356 deletions
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import csv
from copy import deepcopy
from openpyxl.workbook.workbook import Workbook
from mirri import rgetattr
from mirri.settings import GROWTH_MEDIA, MIRRI_FIELDS, DATA_DIR, PUBLICATION_FIELDS
from mirri.settings_v1 import GROWTH_MEDIA, MIRRI_FIELDS, DATA_DIR, PUBLICATION_FIELDS
from mirri.io.parsers.mirri_excel import NAGOYA_TRANSLATOR, RESTRICTION_USE_TRANSLATOR
INITIAL_SEXUAL_STATES = [
"Mata",
"Matalpha",
"Mata/Matalpha",
"Mata",
"Matb",
"Mata/Matb",
"MTLa",
"MTLalpha",
"MTLa/MTLalpha",
"MAT1-1",
"MAT1-2",
"MAT1",
"MAT2",
"MT+",
"MT-",
"MT+",
"MT-",
"H+",
"H-",
]
MARKER_FIELDS = [
{"attribute": "acronym", "label": "Acronym", "mandatory": True},
{"attribute": "marker", "label": "Marker", "mandatory": True},
]
MARKER_DATA = [
{"acronym": "16S rRNA", "marker": "16S rRNA"},
{"acronym": "ACT", "marker": "Actin"},
{"acronym": "CaM", "marker": "Calmodulin"},
{"acronym": "EF-1α", "marker": "elongation factor 1-alpha (EF-1α)"},
{"acronym": "ITS", "marker": "nuclear ribosomal Internal Transcribed Spacer (ITS)"},
{"acronym": "LSU", "marker": "nuclear ribosomal Large SubUnit (LSU)"},
{"acronym": "RPB1", "marker": "Ribosomal RNA-coding genes RPB1"},
{"acronym": "RPB2", "marker": "Ribosomal RNA-coding genes RPB2"},
{"acronym": "TUBB", "marker": "β-Tubulin"},
]
REV_RESTRICTION_USE_TRANSLATOR = {v: k for k, v in RESTRICTION_USE_TRANSLATOR.items()}
REV_NAGOYA_TRANSLATOR = {v: k for k, v in NAGOYA_TRANSLATOR.items()}
PUB_HEADERS = [pb["label"] for pb in PUBLICATION_FIELDS]
def write_mirri_excel(path, strains, growth_media, version):
if version == "20200601":
_write_mirri_excel_20200601(path, strains, growth_media)
if version == "12052023":
_write_mirri_excel_12052023(path, strains, growth_media)
def _write_mirri_excel_20200601(path, strains, growth_media):
wb = Workbook()
write_markers_sheet(wb)
ontobiotope_path = DATA_DIR / "ontobiotopes.csv"
write_ontobiotopes(wb, ontobiotope_path)
write_growth_media(wb, growth_media)
growth_media_indexes = [str(gm.acronym) for gm in growth_media]
locations = {}
publications = {}
sexual_states = set(deepcopy(INITIAL_SEXUAL_STATES))
genomic_markers = {}
strains_data = _deserialize_strains(strains, locations, growth_media_indexes,
publications, sexual_states, genomic_markers)
strains_data = list(strains_data)
# write strain to generate indexed data
strain_sheet = wb.create_sheet("Strains")
strain_sheet.append([field["label"] for field in MIRRI_FIELDS])
for strain_row in strains_data:
strain_sheet.append(strain_row)
redimension_cell_width(strain_sheet)
# write locations
loc_sheet = wb.create_sheet("Geographic origin")
loc_sheet.append(["ID", "Country", "Region", "City", "Locality"])
for index, loc_index in enumerate(locations.keys()):
location = locations[loc_index]
row = [index, location.country, location.state, location.municipality,
loc_index]
loc_sheet.append(row)
redimension_cell_width(loc_sheet)
# write publications
pub_sheet = wb.create_sheet("Literature")
pub_sheet.append(PUB_HEADERS)
for publication in publications.values():
row = []
for pub_field in PUBLICATION_FIELDS:
# if pub_field['attribute'] == 'id':
# value = index
value = getattr(publication, pub_field['attribute'], None)
row.append(value)
pub_sheet.append(row)
redimension_cell_width(pub_sheet)
# write sexual states
sex_sheet = wb.create_sheet("Sexual state")
for sex_state in sorted(list(sexual_states)):
sex_sheet.append([sex_state])
redimension_cell_width(sex_sheet)
# write genetic markers
markers_sheet = wb.create_sheet("Genomic information")
markers_sheet.append(['Strain AN', 'Marker', 'INSDC AN', 'Sequence'])
for strain_id, markers in genomic_markers.items():
for marker in markers:
row = [strain_id, marker.marker_type, marker.marker_id, marker.marker_seq]
markers_sheet.append(row)
redimension_cell_width(markers_sheet)
del wb["Sheet"]
wb.save(str(path))
def _write_mirri_excel_12052023(path, strains, growth_media):
wb = Workbook()
write_markers_sheet(wb)
ontobiotope_path = DATA_DIR / "ontobiotopes.csv"
write_ontobiotopes(wb, ontobiotope_path)
write_growth_media(wb, growth_media)
growth_media_indexes = [str(gm.acronym) for gm in growth_media]
locations = {}
publications = {}
sexual_states = set(deepcopy(INITIAL_SEXUAL_STATES))
genomic_markers = {}
strains_data = _deserialize_strains(strains, locations, growth_media_indexes,
publications, sexual_states, genomic_markers)
strains_data = list(strains_data)
# write strain to generate indexed data
strain_sheet = wb.create_sheet("Strains")
strain_sheet.append([field["label"] for field in MIRRI_FIELDS])
for strain_row in strains_data:
strain_sheet.append(strain_row)
redimension_cell_width(strain_sheet)
# write locations
loc_sheet = wb.create_sheet("Geographic origin")
loc_sheet.append(["ID", "Country", "Region", "City", "Locality"])
for index, loc_index in enumerate(locations.keys()):
location = locations[loc_index]
row = [index, location.country, location.state, location.municipality,
loc_index]
loc_sheet.append(row)
redimension_cell_width(loc_sheet)
# write publications
pub_sheet = wb.create_sheet("Literature")
pub_sheet.append(PUB_HEADERS)
for publication in publications.values():
row = []
for pub_field in PUBLICATION_FIELDS:
# if pub_field['attribute'] == 'id':
# value = index
value = getattr(publication, pub_field['attribute'], None)
row.append(value)
pub_sheet.append(row)
redimension_cell_width(pub_sheet)
# write sexual states
sex_sheet = wb.create_sheet("Sexual state")
for sex_state in sorted(list(sexual_states)):
sex_sheet.append([sex_state])
redimension_cell_width(sex_sheet)
# write genetic markers
markers_sheet = wb.create_sheet("Genomic information")
markers_sheet.append(['Strain AN', 'Marker', 'INSDC AN', 'Sequence'])
for strain_id, markers in genomic_markers.items():
for marker in markers:
row = [strain_id, marker.marker_type, marker.marker_id, marker.marker_seq]
markers_sheet.append(row)
redimension_cell_width(markers_sheet)
del wb["Sheet"]
wb.save(str(path))
def _deserialize_strains(strains, locations, growth_media_indexes,
publications, sexual_states, genomic_markers):
for strain in strains:
strain_row = []
for field in MIRRI_FIELDS:
attribute = field["attribute"]
if attribute == "id":
value = strain.id.strain_id
elif attribute == "restriction_on_use":
value = rgetattr(strain, attribute)
if value is not None:
value = REV_RESTRICTION_USE_TRANSLATOR[value]
elif attribute == "nagoya_protocol":
value = rgetattr(strain, attribute)
if value:
value = REV_NAGOYA_TRANSLATOR[value]
elif attribute == "other_numbers":
value = rgetattr(strain, attribute)
if value is not None:
value = [f"{on.collection} {on.number}" for on in value]
value = "; ".join(value)
elif attribute == 'other_denominations':
od = strain.other_denominations
value = "; ".join(od) if od else None
elif attribute in (
"is_from_registered_collection",
"is_subject_to_quarantine",
"is_potentially_harmful",
"genetics.gmo",
"taxonomy.interspecific_hybrid"
):
value = rgetattr(strain, attribute)
if value is True:
value = 2
elif value is False:
value = 1
else:
value = None
elif attribute == "taxonomy.taxon_name":
value = strain.taxonomy.long_name
elif attribute in ("deposit.date", "collect.date", "isolation.date",
'catalog_inclusion_date'):
value = rgetattr(strain, attribute)
value = value.strfdate if value else None
elif attribute == "growth.recommended_media":
value = rgetattr(strain, attribute)
if value is not None:
for gm in value:
gm = str(gm)
if gm not in growth_media_indexes:
print(gm, growth_media_indexes)
msg = f"Growth media {gm} not in the provided ones"
continue
raise ValueError(msg)
value = "/".join(value)
elif attribute in ('growth.tested_temp_range',
"growth.recommended_temp"):
value = rgetattr(strain, attribute)
if value:
value = f'{value["min"]}; {value["max"]}'
elif attribute == "form_of_supply":
value = rgetattr(strain, attribute)
value = ";".join(value)
elif attribute == "collect.location.coords":
lat = strain.collect.location.latitude
long = strain.collect.location.longitude
alt = strain.collect.location.altitude
prec = strain.collect.location.precision
if lat is not None and long is not None and prec is not None and alt is not None:
value = f"{lat};{long};{prec};{alt}"
else:
value = None
elif attribute == "collect.site.links":
name = strain.collect.site.links.nameSite
url = strain.collect.site.links.urlSite
value = rgetattr(strain, attribute)
value = ";".join(value)
if name is not None and url is not None:
value = f"{name};{url}"
else:
value = None
elif attribute == "collect.location":
location = strain.collect.location
loc_index = _build_location_index(location)
if loc_index is None:
continue
if loc_index not in locations:
locations[loc_index] = location
value = loc_index
elif attribute in ("abs_related_files", "mta_files"):
value = rgetattr(strain, attribute)
value = ";".join(value) if value else None
elif attribute == "taxonomy.organism_type":
value = rgetattr(strain, attribute)
if value:
value = "; ".join([str(v.code) for v in value])
elif attribute == "history":
value = rgetattr(strain, attribute)
if value is not None:
value = " < ".join(value)
elif attribute == "genetics.sexual_state":
value = rgetattr(strain, attribute)
if value:
sexual_states.add(value)
elif attribute == "genetics.ploidy":
value = rgetattr(strain, attribute)
elif attribute == "taxonomy.organism_type":
organism_types = rgetattr(strain, attribute)
if organism_types is not None:
value = [org_type.code for org_type in organism_types]
value = ";".join(value)
elif attribute == 'publications':
value = []
for pub in strain.publications:
value.append(pub.id)
if pub.id not in publications:
publications[pub.id] = pub
value = ';'.join(str(v) for v in value) if value else None
elif attribute == 'genetics.plasmids':
value = rgetattr(strain, attribute)
if value is not None:
value = ';'.join(value)
else:
value = rgetattr(strain, attribute)
strain_row.append(value)
genomic_markers[strain.id.strain_id] = strain.genetics.markers
yield strain_row
def _build_location_index(location):
index = []
if location.country:
index.append(location.country)
if location.site:
index.append(location.site)
return ';'.join(index) if index else None
def write_markers_sheet(wb):
sheet = wb.create_sheet("Markers")
_write_work_sheet(
sheet,
labels=[f["label"] for f in MARKER_FIELDS],
attributes=[f["attribute"] for f in MARKER_FIELDS],
data=MARKER_DATA,
)
redimension_cell_width(sheet)
def write_ontobiotopes(workbook, ontobiotype_path):
ws = workbook.create_sheet("Ontobiotope")
with ontobiotype_path.open() as fhand:
for row in csv.reader(fhand, delimiter="\t"):
ws.append(row)
redimension_cell_width(ws)
def _write_work_sheet(sheet, labels, attributes, data):
sheet.append(labels)
for row in data:
row_data = [row[field] for field in attributes]
sheet.append(row_data)
redimension_cell_width(sheet)
def write_growth_media(wb, growth_media):
ws = wb.create_sheet(GROWTH_MEDIA)
ws.append(["Acronym", "Description", "Full description"])
for growth_medium in growth_media:
row = [
growth_medium.acronym,
growth_medium.description,
growth_medium.full_description,
]
ws.append(row)
redimension_cell_width(ws)
def redimension_cell_width(ws):
dims = {}
for row in ws.rows:
for cell in row:
if cell.value:
max_ = max((dims.get(cell.column_letter, 0), len(str(cell.value))))
dims[cell.column_letter] = max_
for col, value in dims.items():
ws.column_dimensions[col].width = value