jgi-lakehouse

SKILL.md

JGI Lakehouse Skill

Quick Start

What is it? JGI's unified data warehouse (651 tables) + filesystem access to genome files.

Two data access methods:

  1. Lakehouse (Dremio) → Metadata, annotations, taxonomy (no sequences)
  2. JGI Filesystem → Actual genome files (FNA, FAA, GFF) via taxon OID

SQL Dialect: ANSI SQL (not PostgreSQL)

  • Use CAST(x AS type) not ::
  • Use REGEXP_LIKE() not ~
  • Identifiers with dashes need double quotes: "gold-db-2 postgresql"
-- Quick test
SELECT gold_id, project_name FROM "gold-db-2 postgresql".gold.project
WHERE is_public = 'Yes' LIMIT 5;

When to Use

  • Query JGI genomics metadata (GOLD, IMG, Mycocosm, Phytozome)
  • Find genomes and/or metagenomes by taxonomy, ecosystem, or phenotype.
  • Download microbial genomes with IMG taxon OIDs
  • Cross-reference GOLD projects with IMG annotations

Data Access: Lakehouse vs Filesystem

Need Source Access Method
Metadata (taxonomy, projects) Lakehouse SQL via REST API
Gene annotations (COG, Pfam, KO) Lakehouse SQL via REST API
Genome sequences (FNA) JGI Filesystem Copy from /clusterfs/jgi/img_merfs-ro/
Protein sequences (FAA) JGI Filesystem Copy from /clusterfs/jgi/img_merfs-ro/
Metagenome proteins only Lakehouse numg-iceberg.faa table

Critical insight: The Lakehouse is a METADATA warehouse. Genome sequences must be accessed from the JGI filesystem.


Key Data Sources

Source Path Contents
GOLD "gold-db-2 postgresql".gold.* Projects, studies, samples, taxonomy
IMG "img-db-2 postgresql".img_core_v400.* Taxons, genes, annotations (244 tables)
Portal "portal-db-1".portal.* Download tracking, file paths
Mycocosm "myco-db-1 mysql".<organism>.* Fungal genomes (2,711 schemas)
Phytozome "plant-db-7 postgresql".* Plant genomics
NUMG "numg-iceberg"."numg-iceberg".* Metagenome proteins, Pfam hits

Full table catalog: See docs/data-catalog.md


NUMG (Metagenome Proteins) Agent Workflow

Use NUMG when the task is metagenome protein sequence/domain analysis.

Scope rules:

  • numg-iceberg is metagenome-focused.
  • Do not use NUMG for isolate genome protein retrieval; use IMG filesystem packages.

Core tables:

  • "numg-iceberg"."numg-iceberg".faa
    • oid, gene_oid, faa (protein sequence)
  • "numg-iceberg"."numg-iceberg".gene2pfam
    • oid, gene_oid, pfam, evalue, alignment coordinate fields

Recommended query flow:

-- 1) Confirm available NUMG tables
SHOW TABLES IN "numg-iceberg"."numg-iceberg";

-- 2) Inspect schema before writing joins/filters
DESCRIBE "numg-iceberg"."numg-iceberg".faa;
DESCRIBE "numg-iceberg"."numg-iceberg".gene2pfam;

-- 3) Domain filter (use exact lowercase pfam IDs)
SELECT oid, gene_oid, pfam, evalue
FROM "numg-iceberg"."numg-iceberg".gene2pfam
WHERE pfam IN ('pfam00001', 'pfam00004')
LIMIT 100;

-- 4) Join domains to protein sequences
SELECT
  p.oid,
  p.gene_oid,
  p.pfam,
  p.evalue,
  f.faa
FROM "numg-iceberg"."numg-iceberg".gene2pfam p
JOIN "numg-iceberg"."numg-iceberg".faa f
  ON p.oid = f.oid
 AND p.gene_oid = f.gene_oid
WHERE p.pfam = 'pfam00001'
LIMIT 100;

Important NUMG rules:

  • Join on both oid and gene_oid (not gene_oid alone).
  • Keep Pfam filters exact (pfam00001, not case-transformed).
  • Always start with LIMIT and expand only after verifying row shape.

See also: examples/05-query-numg-metagenome-proteins.md


Downloading Genomes with IMG Taxon OIDs

Option 1: JGI Filesystem (Fastest)

# Genome packages are at:
/clusterfs/jgi/img_merfs-ro/img_web/img_web_data/download/{taxon_oid}.tar.gz

# Example: Copy and extract
cp /clusterfs/jgi/img_merfs-ro/img_web/img_web_data/download/8136918376.tar.gz .
tar -xzf 8136918376.tar.gz

Package contents:

  • {taxon_oid}.fna - Genome assembly
  • {taxon_oid}.genes.faa - Protein sequences
  • {taxon_oid}.genes.fna - Gene nucleotide sequences
  • {taxon_oid}.gff - GFF annotations
  • {taxon_oid}.cog.tab.txt - COG annotations
  • {taxon_oid}.pfam.tab.txt - Pfam annotations
  • {taxon_oid}.ko.tab.txt - KEGG KO annotations

Portal Downloads (Mycocosm / Phytozome)

The portal tracks downloadable files for Mycocosm and Phytozome in "portal-db-1".portal.downloadRequestFiles. Use filePath to copy data from the JGI filesystem (/global/dna/dm_archive/...).

Mycocosm (fungal genomes/proteins):

SELECT filePath, fileType
FROM "portal-db-1".portal.downloadRequestFiles
WHERE LOWER(filePath) LIKE '%mycocosm%'
  AND (filePath LIKE '%.fasta%' OR filePath LIKE '%.fa%' OR filePath LIKE '%.faa%')
LIMIT 20;

Phytozome (plant genomes/proteins):

SELECT filePath, fileType
FROM "portal-db-1".portal.downloadRequestFiles
WHERE LOWER(filePath) LIKE '%phytozome%'
  AND (filePath LIKE '%.fa%' OR filePath LIKE '%.fna%' OR filePath LIKE '%.faa%')
LIMIT 20;

Download from filesystem:

cp /global/dna/dm_archive/<path/from-filePath> .

Notes:

  • fileType typically includes Assembly, Annotation, or Sequence.
  • virtualPath can provide a user-facing download label but filePath is the real location.

Query Best Practices

⚠️ CRITICAL: When building queries, distinguish between exploration and comprehensive analysis:

Exploration Queries

Use LIMIT for quick validation during development:

-- For testing query structure and results
SELECT gold_id, project_name
FROM "gold-db-2 postgresql".gold.project
WHERE is_public = 'Yes'
LIMIT 10;  -- ✓ OK for testing

Comprehensive Queries

Remove LIMIT and other result-limiting clauses when answering actual questions:

-- For getting actual dataset counts/results
SELECT COUNT(DISTINCT taxon_oid)
FROM "img-db-2 postgresql".img_core_v400.taxon
WHERE genome_type = 'metagenome'
  AND is_public = 'Yes';
-- ✓ No LIMIT - gets true total

Common pitfalls:

  • LIMIT 100 on initial exploration → assumes only 100 results exist
  • LIMIT 50 on a "find all" query → misses 99% of data
  • ❌ Using FETCH FIRST N ROWS → same issue as LIMIT

Best practice:

  1. Use LIMIT with COUNT(*) or small LIMIT during development
  2. Once query logic is correct, remove LIMIT to get true results
  3. For very large result sets, use aggregation (COUNT, GROUP BY) to summarize instead

Common Queries

Find Bacterial Isolate Genomes

-- Get count of all finished bacterial isolates
SELECT COUNT(DISTINCT taxon_oid) as total_isolates
FROM "img-db-2 postgresql".img_core_v400.taxon
WHERE domain = 'Bacteria'
  AND genome_type = 'isolate'
  AND is_public = 'Yes'
  AND seq_status = 'Finished';

-- Get sample of isolates (if you need details)
SELECT taxon_oid, taxon_display_name, phylum, genus, species
FROM "img-db-2 postgresql".img_core_v400.taxon
WHERE domain = 'Bacteria'
  AND genome_type = 'isolate'
  AND is_public = 'Yes'
  AND seq_status = 'Finished'
LIMIT 100;

Link GOLD Project to IMG Taxon

SELECT COUNT(DISTINCT t.taxon_oid) as total_linked
FROM "img-db-2 postgresql".img_core_v400.taxon t
WHERE t.sequencing_gold_id IS NOT NULL;

Find Genomes with File Paths (Portal)

SELECT COUNT(DISTINCT taxonOid) as total_tar_gz
FROM "portal-db-1".portal.downloadRequestFiles
WHERE taxonOid IS NOT NULL
  AND filePath LIKE '%.tar.gz';

Critical Pitfalls

Wrong Correct
Using LIMIT in comprehensive queries Remove LIMIT when answering actual questions; use COUNT() for aggregation
Join ncbi_assembly on project_id ncbi_assembly has no project_id; use bioproject or biosample
project.ecosystem Join study via master_study_id
SHOW SCHEMAS IN "source" Works, but some syntax errors in older Dremio
Get sequences from Lakehouse Download from JGI filesystem
sra_experiment_v2.platform Use library_instrument
gene_ko_terms = 'K00025' Use gene_ko_terms = 'KO:K00025'
Join NUMG on gene_oid only Join on both oid and gene_oid
Case-normalizing large function tables Use exact normalized values (pfam00001, COG1389, etc.)
Isolate benchmark counts vary Add obsolete_flag = 'No' and is_public = 'Yes'
IMG.gene_feature fails expansion Fallback to "img-db-2 postgresql".img_core_v400.* tables
show_schemas() misses sources Use higher limit (e.g. show_schemas(limit=2000))

Authentication

export DREMIO_PAT=$(cat ~/.secrets/dremio_pat)

Token setup: See docs/authentication.md


API Access

REST API Base: http://lakehouse-1.jgi.lbl.gov:9047/api/v3

# Use scripts/rest_client.py
from rest_client import query
results = query("SELECT * FROM ... LIMIT 10")

Arrow Flight (Python)

For higher-performance programmatic access, use Arrow Flight with Python.

python3 -m venv venv
. venv/bin/activate
pip install \
  https://github.com/dremio-hub/arrow-flight-client-examples/releases/download/dremio-flight-python-v1.1.0/dremio_flight-1.1.0-py3-none-any.whl

Full guide: docs/arrow-flight-python.md


Documentation

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