Genophenocorr is a Python library for genotype-phenotype association analysis.

An example of simple genotype-phenotype association analysis

# Load HPO
import hpotk

store = hpotk.configure_ontology_store()
hpo = store.load_minimal_hpo()

# Load a cohort of phenopackets
from genophenocorr.data import get_toy_cohort

cohort = get_toy_cohort()

# Analyze genotype-phenotype associations
from genophenocorr.analysis import configure_cohort_analysis
from genophenocorr.analysis.predicate import PatientCategories

from genophenocorr.model import VariantEffect

cohort_analysis = configure_cohort_analysis(cohort, hpo)
frameshift = cohort_analysis.compare_by_variant_effect(VariantEffect.FRAMESHIFT_VARIANT, tx_id='NM_1234.5')

frameshift.summarize(hpo, category=PatientCategories.YES)

provides a pandas data frame with genotype-phenotype correlations:

FRAMESHIFT_VARIANT on NM_1234.5                                    No                Yes
                                                                Count   Percent    Count   Percent    p value    Corrected p value
    Arachnodactyly [HP:0001166]                                  1/10       10%    13/16       81%   0.000781             0.020299
    Abnormality of the musculature [HP:0003011]                   6/6      100%    11/11      100%   1.000000             1.000000
    Abnormal nervous system physiology [HP:0012638]               9/9      100%    15/15      100%   1.000000             1.000000
    ...                                                           ...       ...      ...       ...        ...                  ...

Documentation

Check out the User guide and the API reference for more info:

• Stable documentation (last release on main branch)
• Latest documentation (bleeding edge, latest commit on development branch)