Aggregation Operators
Aggregation operators combine and cluster genomic intervals. These operators are essential for reducing complex interval data into summarized regions, such as merging overlapping peaks or identifying clusters of related features.
CLUSTER
Assign cluster IDs to overlapping or nearby genomic intervals.
Description
The CLUSTER operator assigns a unique cluster identifier to groups of intervals
that overlap or are within a specified distance of each other. Intervals in the same
cluster share a common cluster ID, while non-overlapping intervals receive different
IDs.
This is useful for:
Grouping overlapping features
Identifying regions of high feature density
Preparing data for downstream merge operations
Syntax
-- Basic clustering (overlapping intervals)
CLUSTER(interval) AS cluster_id
-- Clustering with distance parameter
CLUSTER(interval, distance) AS cluster_id
-- Strand-specific clustering
CLUSTER(interval, stranded=true) AS cluster_id
-- Combined parameters
CLUSTER(interval, distance, stranded=true) AS cluster_id
Parameters
- interval
A genomic column registered with the engine.
- distance (optional)
Maximum gap between intervals to consider them part of the same cluster. Default:
0(only overlapping intervals are clustered).- stranded (optional)
When
true, only cluster intervals on the same strand. Default:false.
Return Value
Integer cluster ID. Intervals in the same cluster have the same ID.
IDs are assigned per-chromosome (and per-strand if stranded=true).
Examples
Basic Clustering:
Assign cluster IDs to overlapping intervals:
cursor = engine.execute("""
SELECT
*,
CLUSTER(interval) AS cluster_id
FROM features
ORDER BY chromosome, start_pos
""")
Distance-Based Clustering:
Cluster intervals within 1000bp of each other:
cursor = engine.execute("""
SELECT
*,
CLUSTER(interval, 1000) AS cluster_id
FROM features
ORDER BY chromosome, start_pos
""")
Strand-Specific Clustering:
Cluster intervals separately by strand:
cursor = engine.execute("""
SELECT
*,
CLUSTER(interval, stranded=true) AS cluster_id
FROM features
ORDER BY chromosome, strand, start_pos
""")
Analyze Cluster Statistics:
Count features per cluster:
cursor = engine.execute("""
WITH clustered AS (
SELECT
*,
CLUSTER(interval) AS cluster_id
FROM features
)
SELECT
chromosome,
cluster_id,
COUNT(*) AS feature_count,
MIN(start_pos) AS cluster_start,
MAX(end_pos) AS cluster_end
FROM clustered
GROUP BY chromosome, cluster_id
ORDER BY chromosome, cluster_start
""")
Filter by Cluster Size:
Find regions with multiple overlapping features:
cursor = engine.execute("""
WITH clustered AS (
SELECT
*,
CLUSTER(interval) AS cluster_id
FROM features
),
cluster_sizes AS (
SELECT cluster_id, COUNT(*) AS size
FROM clustered
GROUP BY cluster_id
)
SELECT c.*
FROM clustered c
INNER JOIN cluster_sizes s ON c.cluster_id = s.cluster_id
WHERE s.size >= 3
""")
Backend Compatibility
Backend |
Support |
Notes |
|---|---|---|
DuckDB |
Full |
Efficient window function implementation |
SQLite |
Full |
|
PostgreSQL |
Planned |
Performance Notes
Data should be sorted by chromosome and position for efficient clustering
For large datasets, consider partitioning by chromosome
Cluster IDs are computed using window functions, which scale well
MERGE
Combine overlapping genomic intervals into unified regions.
Description
The MERGE operator combines overlapping (or nearby) intervals into single,
non-overlapping regions. This is useful for:
Creating consensus regions from overlapping features
Reducing redundant annotations
Calculating total coverage
The operator works as an aggregate function, returning one row per merged region with the unified coordinates.
Syntax
-- Basic merge
SELECT MERGE(interval) FROM features
-- Merge with distance parameter
SELECT MERGE(interval, distance) FROM features
-- Strand-specific merge
SELECT MERGE(interval, stranded=true) FROM features
-- Merge with additional aggregations
SELECT
MERGE(interval),
COUNT(*) AS feature_count,
AVG(score) AS avg_score
FROM features
Parameters
- interval
A genomic column registered with the engine.
- distance (optional)
Maximum gap between intervals to merge. Default:
0(only overlapping intervals are merged).- stranded (optional)
When
true, merge intervals separately by strand. Default:false.
Return Value
Returns merged interval coordinates:
chromosome- Chromosome of the merged regionstart_pos- Start position of the merged regionend_pos- End position of the merged regionstrand- Strand (ifstranded=true)
Examples
Basic Merge:
Merge all overlapping intervals:
cursor = engine.execute("""
SELECT MERGE(interval)
FROM features
""")
# Returns: chromosome, start_pos, end_pos for each merged region
Distance-Based Merge:
Merge intervals within 1000bp of each other:
cursor = engine.execute("""
SELECT MERGE(interval, 1000)
FROM features
""")
Strand-Specific Merge:
Merge intervals separately by strand:
cursor = engine.execute("""
SELECT MERGE(interval, stranded=true)
FROM features
""")
Merge with Feature Count:
Count how many features were merged into each region:
cursor = engine.execute("""
SELECT
MERGE(interval),
COUNT(*) AS feature_count
FROM features
""")
Merge with Aggregations:
Calculate statistics for merged regions:
cursor = engine.execute("""
SELECT
MERGE(interval),
COUNT(*) AS feature_count,
AVG(score) AS avg_score,
MAX(score) AS max_score
FROM features
""")
Collect Merged Feature Names:
List the names of features that were merged:
cursor = engine.execute("""
SELECT
MERGE(interval),
STRING_AGG(name, ',') AS feature_names
FROM features
""")
Merge by Chromosome:
Process each chromosome separately (explicit grouping):
cursor = engine.execute("""
SELECT
chromosome,
MERGE(interval),
COUNT(*) AS feature_count
FROM features
GROUP BY chromosome
ORDER BY chromosome
""")
Calculate Total Coverage:
Calculate the total base pairs covered after merging:
cursor = engine.execute("""
WITH merged AS (
SELECT MERGE(interval) AS merged_pos
FROM features
)
SELECT SUM(end_pos - start_pos) AS total_coverage
FROM merged
""")
Backend Compatibility
Backend |
Support |
Notes |
|---|---|---|
DuckDB |
Full |
|
SQLite |
Full |
|
PostgreSQL |
Planned |
Performance Notes
MERGE is an aggregate operation that processes all matching rows
For very large datasets, consider filtering by chromosome first
The operation sorts data internally, so pre-sorting is not required
Related Operators
CLUSTER - Assign cluster IDs without merging
INTERSECTS - Test for overlap between specific pairs