Added additional test for fully automatic typing based on sequence
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@ -1,6 +1,6 @@
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from os import path
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from typing import Any, AsyncGenerator, AsyncIterable, Iterable, Sequence
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from automlst.engine.data.MLST import MLSTProfile
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from automlst.engine.data.mlst import MLSTProfile
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from automlst.engine.data.genomics import NamedString
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from automlst.engine.local.abif import read_abif
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from automlst.engine.local.fasta import read_fasta
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@ -3,7 +3,7 @@ from io import TextIOWrapper
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from os import PathLike
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from typing import AsyncIterable, Iterable, Mapping, Sequence, Union
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from automlst.engine.data.MLST import Allele, MLSTProfile
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from automlst.engine.data.mlst import Allele, MLSTProfile
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def loci_alleles_variants_from_loci(alleles_map: Mapping[str, Sequence[Allele]]):
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@ -3,7 +3,7 @@ from contextlib import AbstractAsyncContextManager
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import re
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from typing import Any, AsyncGenerator, AsyncIterable, Generator, Iterable, Sequence, Union
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from aiohttp import ClientSession, ClientTimeout
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from automlst.engine.data.MLST import Allele, MLSTProfile
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from automlst.engine.data.mlst import Allele, MLSTProfile
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from automlst.engine.data.genomics import NamedString
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class InstitutPasteurProfiler(AbstractAsyncContextManager):
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@ -4,7 +4,7 @@ from typing import AsyncGenerator, AsyncIterable, Generator, Iterable, Mapping,
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from aiohttp import ClientSession
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from automlst.engine.data.MLST import Allele, MLSTProfile
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from automlst.engine.data.mlst import Allele, MLSTProfile
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MLST_DATABASES = [
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"https://bigsdb.pasteur.fr/api/db",
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@ -3,7 +3,7 @@ from contextlib import AbstractAsyncContextManager
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import re
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from typing import Any, AsyncGenerator, AsyncIterable, Generator, Iterable, Mapping, Sequence, Union
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from aiohttp import ClientSession, ClientTimeout
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from automlst.engine.data.MLST import Allele, MLSTProfile
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from automlst.engine.data.mlst import Allele, MLSTProfile
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from automlst.engine.data.genomics import NamedString
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from automlst.engine.remote.databases.mlst import MLSTProfiler
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@ -1,5 +1,5 @@
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from Bio import SeqIO
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from automlst.engine.data.MLST import Allele, MLSTProfile
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from automlst.engine.data.mlst import Allele, MLSTProfile
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from automlst.engine.remote.databases.institutpasteur.mlst import InstitutPasteurProfiler
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@ -32,4 +32,22 @@ async def test_profiling_results_in_correct_st():
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assert mlst_st_data is not None
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assert isinstance(mlst_st_data, MLSTProfile)
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assert mlst_st_data.clonal_complex == "ST-2 complex"
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assert mlst_st_data.sequence_type == "1"
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assert mlst_st_data.sequence_type == "1"
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async def test_sequence_profiling_is_correct():
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sequence = str(SeqIO.read("tests/resources/tohama_I_bpertussis.fasta", "fasta").seq)
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dummy_alleles = [
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Allele("adk", "1"),
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Allele("fumC", "1"),
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Allele("glyA", "1"),
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Allele("tyrB", "1"),
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Allele("icd", "1"),
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Allele("pepA", "1"),
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Allele("pgm", "1"),
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]
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async with InstitutPasteurProfiler(database_name="pubmlst_bordetella_seqdef") as dummy_profiler:
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profile = await dummy_profiler.profile_string(sequence)
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assert profile is not None
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assert isinstance(profile, MLSTProfile)
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assert profile.clonal_complex == "ST-2 complex"
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assert profile.sequence_type == "1"
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