feat: gwas catalog top-hit + study step

docs/python_api/steps/gwas_catalog_study_index.md

@@ -0,0 +1,5 @@
+---
+title: gwas_catalog_study_inclusion
+---
+
+::: gentropy.gwas_catalog_study_index.GWASCatalogStudyIndexGenerationStep

docs/python_api/steps/gwas_catalog_top_hits.md

@@ -0,0 +1,5 @@
+---
+title: GWAS Catalog Top Hits Ingestion Step
+---
+
+::: gentropy.gwas_catalog_top_hits.GWASCatalogTopHitIngestionStep

src/gentropy/assets/schemas/study_index.json

@@ -264,33 +264,12 @@
       "metadata": {}
     },
     {
-      "name": "sumStatQCPerformed",
-      "type": "boolean",
-      "nullable": true,
-      "metadata": {}
-    },
-    {
-      "name": "sumStatQCValues",
+      "name": "sumstatQCValues",
       "type": {
-        "type": "array",
-        "elementType": {
-          "type": "struct",
-          "fields": [
-            {
-              "name": "QCCheckName",
-              "type": "string",
-              "nullable": true,
-              "metadata": {}
-            },
-            {
-              "name": "QCCheckValue",
-              "type": "float",
-              "nullable": true,
-              "metadata": {}
-            }
-          ]
-        },
-        "containsNull": true
+        "type": "map",
+        "keyType": "string",
+        "valueType": "float",
+        "valueContainsNull": true
       },
       "nullable": true,
       "metadata": {}

src/gentropy/config.py

@@ -68,44 +68,36 @@ class GWASCatalogStudyCurationConfig(StepConfig):
 
     catalog_study_files: list[str] = MISSING
     catalog_ancestry_files: list[str] = MISSING
-    catalog_sumstats_lut: str = MISSING
     gwas_catalog_study_curation_out: str = MISSING
     gwas_catalog_study_curation_file: str = MISSING
     _target_: str = "gentropy.gwas_catalog_study_curation.GWASCatalogStudyCurationStep"
 
 
 @dataclass
-class GWASCatalogStudyInclusionConfig(StepConfig):
-    """GWAS Catalog study inclusion step configuration."""
+class GWASCatalogStudyIndexGenerationStep(StepConfig):
+    """GWAS Catalog study index generation."""
 
     catalog_study_files: list[str] = MISSING
     catalog_ancestry_files: list[str] = MISSING
-    catalog_associations_file: str = MISSING
-    gwas_catalog_study_curation_file: str = MISSING
-    variant_annotation_path: str = MISSING
-    harmonised_study_file: str = MISSING
-    criteria: str = MISSING
-    inclusion_list_path: str = MISSING
-    exclusion_list_path: str = MISSING
+    study_index_path: str = MISSING
+    gwas_catalog_study_curation_file: str | None = None
+    sumstats_qc_path: str | None = None
     _target_: str = (
-        "gentropy.gwas_catalog_study_inclusion.GWASCatalogStudyInclusionGenerator"
+        "gentropy.gwas_catalog_study_index.GWASCatalogStudyIndexGenerationStep"
     )
 
 
 @dataclass
-class GWASCatalogIngestionConfig(StepConfig):
+class GWASCatalogTopHitIngestionConfig(StepConfig):
     """GWAS Catalog ingestion step configuration."""
 
     catalog_study_files: list[str] = MISSING
     catalog_ancestry_files: list[str] = MISSING
-    catalog_sumstats_lut: str = MISSING
     catalog_associations_file: str = MISSING
     variant_annotation_path: str = MISSING
     catalog_studies_out: str = MISSING
     catalog_associations_out: str = MISSING
-    gwas_catalog_study_curation_file: str | None = None
-    inclusion_list_path: str | None = None
-    _target_: str = "gentropy.gwas_catalog_ingestion.GWASCatalogIngestionStep"
+    _target_: str = "gentropy.gwas_catalog_top_hits.GWASCatalogTopHitIngestionStep"
 
 
 @dataclass
@@ -658,17 +650,19 @@ def register_config() -> None:
     )
     cs.store(
         group="step",
-        name="gwas_catalog_study_inclusion",
-        node=GWASCatalogStudyInclusionConfig,
-    )
-    cs.store(
-        group="step", name="gwas_catalog_ingestion", node=GWASCatalogIngestionConfig
+        name="gwas_catalog_study_index",
+        node=GWASCatalogStudyIndexGenerationStep,
     )
     cs.store(
         group="step",
         name="gwas_catalog_sumstat_preprocess",
         node=GWASCatalogSumstatsPreprocessConfig,
     )
+    cs.store(
+        group="step",
+        name="gwas_catalog_top_hit_ingestion",
+        node=GWASCatalogTopHitIngestionConfig,
+    )
     cs.store(group="step", name="ld_based_clumping", node=LDBasedClumpingConfig)
     cs.store(group="step", name="ld_index", node=LDIndexConfig)
     cs.store(group="step", name="locus_to_gene", node=LocusToGeneConfig)

src/gentropy/dataset/study_index.py

@@ -13,6 +13,7 @@
 
 from gentropy.assets import data
 from gentropy.common.schemas import parse_spark_schema
+from gentropy.common.spark_helpers import convert_from_wide_to_long
 from gentropy.dataset.dataset import Dataset
 
 if TYPE_CHECKING:
@@ -32,13 +33,29 @@ class StudyQualityCheck(Enum):
         UNKNOWN_STUDY_TYPE (str): Indicating the provided type of study is not supported.
         UNKNOWN_BIOSAMPLE (str): Flagging if a biosample identifier is not found in the reference.
         DUPLICATED_STUDY (str): Flagging if a study identifier is not unique.
+        SUMSTATS_NOT_AVAILABLE (str): Flagging if harmonized summary statistics are not available or empty.
+        NO_OT_CURATION (str): Flagging if a study has not been curated by Open Targets.
+        FAILED_MEAN_BETA_CHECK (str): Flagging if the mean beta QC check value is not within the expected range.
+        FAILED_PZ_CHECK (str): Flagging if the PZ QC check values are not within the expected range.
+        FAILED_GC_LAMBDA_CHECK (str): Flagging if the GC lambda value is not within the expected range.
+        SMALL_NUMBER_OF_SNPS (str): Flagging if the number of SNPs in the study is below the expected threshold.
     """
 
-    UNRESOLVED_TARGET = "Target/gene identifier could not match to reference."
-    UNRESOLVED_DISEASE = "No valid disease identifier found."
-    UNKNOWN_STUDY_TYPE = "This type of study is not supported."
-    UNKNOWN_BIOSAMPLE = "Biosample identifier was not found in the reference."
-    DUPLICATED_STUDY = "The identifier of this study is not unique."
+    UNRESOLVED_TARGET = "Target/gene identifier could not match to reference"
+    UNRESOLVED_DISEASE = "No valid disease identifier found"
+    UNKNOWN_STUDY_TYPE = "This type of study is not supported"
+    UNKNOWN_BIOSAMPLE = "Biosample identifier was not found in the reference"
+    DUPLICATED_STUDY = "The identifier of this study is not unique"
+    SUMSTATS_NOT_AVAILABLE = "Harmonized summary statistics are not available or empty"
+    NO_OT_CURATION = "GWAS Catalog study has not been curated by Open Targets"
+    FAILED_MEAN_BETA_CHECK = (
+        "The mean beta QC check value is not within the expected range"
+    )
+    FAILED_PZ_CHECK = "The PZ QC check values are not within the expected range"
+    FAILED_GC_LAMBDA_CHECK = "The GC lambda value is not within the expected range"
+    SMALL_NUMBER_OF_SNPS = (
+        "The number of SNPs in the study is below the expected threshold"
+    )
 
 
 @dataclass
@@ -410,7 +427,9 @@ def validate_target(self: StudyIndex, target_index: GeneIndex) -> StudyIndex:
 
         return StudyIndex(_df=validated_df, _schema=StudyIndex.get_schema())
 
-    def validate_biosample(self: StudyIndex, biosample_index: BiosampleIndex) -> StudyIndex:
+    def validate_biosample(
+        self: StudyIndex, biosample_index: BiosampleIndex
+    ) -> StudyIndex:
         """Validating biosample identifiers in the study index against the provided biosample index.
 
         Args:
@@ -419,7 +438,9 @@ def validate_biosample(self: StudyIndex, biosample_index: BiosampleIndex) -> Stu
         Returns:
             StudyIndex: where non-gwas studies are flagged if biosampleIndex could not be validated.
         """
-        biosample_set = biosample_index.df.select("biosampleId", f.lit(True).alias("isIdFound"))
+        biosample_set = biosample_index.df.select(
+            "biosampleId", f.lit(True).alias("isIdFound")
+        )
 
         # If biosampleId in df, we need to drop it:
         if "biosampleId" in self.df.columns:
@@ -430,7 +451,11 @@ def validate_biosample(self: StudyIndex, biosample_index: BiosampleIndex) -> Stu
             return self
 
         validated_df = (
-            self.df.join(biosample_set, self.df.biosampleFromSourceId == biosample_set.biosampleId, how="left")
+            self.df.join(
+                biosample_set,
+                self.df.biosampleFromSourceId == biosample_set.biosampleId,
+                how="left",
+            )
             .withColumn(
                 "isIdFound",
                 f.when(
@@ -450,3 +475,118 @@ def validate_biosample(self: StudyIndex, biosample_index: BiosampleIndex) -> Stu
         )
 
         return StudyIndex(_df=validated_df, _schema=StudyIndex.get_schema())
+
+    def annotate_sumstats_qc(
+        self: StudyIndex,
+        sumstats_qc: DataFrame,
+        threshold_mean_beta: float = 0.05,
+        threshold_mean_diff_pz: float = 0.05,
+        threshold_se_diff_pz: float = 0.05,
+        threshold_min_gc_lambda: float = 0.7,
+        threshold_max_gc_lambda: float = 2.5,
+        threshold_min_n_variants: int = 2_000_000,
+    ) -> StudyIndex:
+        """Annotate summary stats QC information.
+
+        Args:
+            sumstats_qc (DataFrame): containing summary statistics-based quality controls.
+            threshold_mean_beta (float): Threshold for mean beta check. Defaults to 0.05.
+            threshold_mean_diff_pz (float): Threshold for mean diff PZ check. Defaults to 0.05.
+            threshold_se_diff_pz (float): Threshold for SE diff PZ check. Defaults to 0.05.
+            threshold_min_gc_lambda (float): Minimum threshold for GC lambda check. Defaults to 0.7.
+            threshold_max_gc_lambda (float): Maximum threshold for GC lambda check. Defaults to 2.5.
+            threshold_min_n_variants (int): Minimum number of variants for SuSiE check. Defaults to 2_000_000.
+
+        Returns:
+            StudyIndex: Updated study index with QC information
+        """
+        # convert all columns in sumstats_qc dataframe in array of structs grouped by studyId
+        cols = [c for c in sumstats_qc.columns if c != "studyId"]
+
+        studies = self.df
+
+        melted_df = convert_from_wide_to_long(
+            sumstats_qc,
+            id_vars=["studyId"],
+            value_vars=cols,
+            var_name="QCCheckName",
+            value_name="QCCheckValue",
+        )
+
+        qc_df = (
+            melted_df.groupBy("studyId")
+            .agg(
+                f.map_from_entries(
+                    f.collect_list(
+                        f.struct(f.col("QCCheckName"), f.col("QCCheckValue"))
+                    )
+                ).alias("sumStatQCValues")
+            )
+            .select("studyId", "sumstatQCValues")
+        )
+
+        df = (
+            studies.drop("sumStatQCValues", "hasSumstats")
+            .join(
+                qc_df.withColumn("hasSumstats", f.lit(True)), how="left", on="studyId"
+            )
+            .withColumn("hasSumstats", f.coalesce(f.col("hasSumstats"), f.lit(False)))
+            .withColumn(
+                "qualityControls",
+                StudyIndex.update_quality_flag(
+                    f.col("qualityControls"),
+                    ~f.col("hasSumstats"),
+                    StudyQualityCheck.SUMSTATS_NOT_AVAILABLE,
+                ),
+            )
+            .withColumn(
+                "qualityControls",
+                StudyIndex.update_quality_flag(
+                    f.col("qualityControls"),
+                    ~(f.abs(f.col("sumstatQCValues.mean_beta")) <= threshold_mean_beta),
+                    StudyQualityCheck.FAILED_MEAN_BETA_CHECK,
+                ),
+            )
+            .withColumn(
+                "qualityControls",
+                StudyIndex.update_quality_flag(
+                    f.col("qualityControls"),
+                    ~(
+                        (
+                            f.abs(f.col("sumstatQCValues.mean_diff_pz"))
+                            <= threshold_mean_diff_pz
+                        )
+                        & (f.col("sumstatQCValues.se_diff_pz") <= threshold_se_diff_pz)
+                    ),
+                    StudyQualityCheck.FAILED_PZ_CHECK,
+                ),
+            )
+            .withColumn(
+                "qualityControls",
+                StudyIndex.update_quality_flag(
+                    f.col("qualityControls"),
+                    ~(
+                        (f.col("sumstatQCValues.gc_lambda") <= threshold_max_gc_lambda)
+                        & (
+                            f.col("sumstatQCValues.gc_lambda")
+                            >= threshold_min_gc_lambda
+                        )
+                    ),
+                    StudyQualityCheck.FAILED_GC_LAMBDA_CHECK,
+                ),
+            )
+            .withColumn(
+                "qualityControls",
+                StudyIndex.update_quality_flag(
+                    f.col("qualityControls"),
+                    (f.col("sumstatQCValues.n_variants") < threshold_min_n_variants),
+                    StudyQualityCheck.SMALL_NUMBER_OF_SNPS,
+                ),
+            )
+        )
+
+        # Annotate study index with QC information:
+        return StudyIndex(
+            _df=df,
+            _schema=StudyIndex.get_schema(),
+        )

src/gentropy/datasource/gwas_catalog/associations.py

@@ -230,7 +230,9 @@ def _map_variants_to_gnomad_variants(
             "chromosome",
             # Calculate the position in Ensembl coordinates for indels:
             GWASCatalogCuratedAssociationsParser.convert_gnomad_position_to_ensembl(
-                f.col("position"), f.col("referenceAllele"), f.col("alternateAllele")
+                f.col("position"),
+                f.col("referenceAllele"),
+                f.col("alternateAllele"),
             ).alias("ensemblPosition"),
             # Keeping GnomAD position:
             "position",
@@ -240,11 +242,7 @@ def _map_variants_to_gnomad_variants(
             "alleleFrequencies",
             variant_index.max_maf().alias("maxMaf"),
         ).join(
-            f.broadcast(
-                gwas_associations_subset.select(
-                    "chromosome", "ensemblPosition"
-                ).distinct()
-            ),
+            gwas_associations_subset.select("chromosome", "ensemblPosition").distinct(),
             on=["chromosome", "ensemblPosition"],
             how="inner",
         )
@@ -253,7 +251,7 @@ def _map_variants_to_gnomad_variants(
         # based on rsIds or allele concordance)
         filtered_associations = (
             gwas_associations_subset.join(
-                f.broadcast(va_subset),
+                va_subset,
                 on=["chromosome", "ensemblPosition"],
                 how="left",
             )
@@ -1108,7 +1106,10 @@ def from_source(
         pvalue_threshold is keeped in sync with the WindowBasedClumpingStep gwas_significance.
         """
         return StudyLocusGWASCatalog(
-            _df=gwas_associations.withColumn(
+            _df=gwas_associations
+            # drop duplicate rows
+            .distinct()
+            .withColumn(
                 "studyLocusId", f.monotonically_increasing_id().cast(StringType())
             )
             .transform(