| name | encode-ccres-database |
| description | Query the ENCODE Registry of cis-Regulatory Elements (cCREs) via the SCREEN GraphQL API, or make custom queries to the ENCODE Portal REST API for experiments and files (ChIP-seq peaks, etc.). Use when you want to query regulatory annotations or raw experimental data across human cell types.
|
ENCODE Database Skill
This skill allows you to query the ENCODE Registry of cCREs (candidate
cis-Regulatory Elements) via the SCREEN GraphQL API. It helps identify
functional non-coding DNA elements (like Promoters, Enhancers, and insulators)
by analyzing biochemical signatures (DNase, H3K4me3, H3K27ac, CTCF).
Prerequisites
uv: Read the uv skill and follow its Setup instructions to ensure
uv is installed and on PATH.
- User Notification: If LICENSE_NOTIFICATION.txt does not already exist in
this skill directory then (1) prominently notify the user to check the terms
at https://www.encodeproject.org/help/rest-api/, then (2) create the file
recording the notification text and timestamp.
Core Rules
- Use the Wrapper: ALWAYS execute the provided helper scripts to query the
database rather than accessing the database directly. The scripts
automatically enforce the required rate limit gracefully.
- Parsing Output: Do NOT use
cat to read the entire JSON output file
into context, as it can be extremely large. You MUST use jq to efficiently
parse and extract relevant fields.
- Notification: If this skill is used, ensure this is mentioned in the
output.
Quick Start
uv run scripts/screen_api.py search --chromosome chr11 \
--start 5205263 --end 5207263 \
--output /tmp/search.json
uv run scripts/screen_api.py details EH38E2941922 \
--output /tmp/details.json
All subcommands write JSON to disk. Always save output in a temporary location
like /tmp/.
Identifying High-Confidence ("Type A") Biosamples
Biosamples in ENCODE are often categorized by their data completeness. "Type
A" (or high-confidence) biosamples are those that have experimental data for
all four core epigenetic markers: DNase, H3K4me3, H3K27ac, and CTCF.
The biosamples and details commands automatically enrich their output with
an is_type_a boolean flag for each biosample.
Example: Finding high-confidence cell types
uv run scripts/screen_api.py biosamples --output /tmp/biosamples.json
jq '.data.ccREBiosampleQuery.biosamples[] | select(.is_type_a == true) | .displayname' /tmp/biosamples.json
Parsing Output (CRITICAL)
Do NOT use cat to read the entire JSON output file into context, as it
can be extremely large. Instead, you MUST use jq to efficiently parse and
extract the relevant fields from the JSON file saved by the script. If jq is
not available on the system, write your own Python filtering code (e.g.,
python3 -c "import json...") to extract the necessary data.
For a complete reference of the JSON structure returned by eachmcommand (so you
know which fields to query with jq), read
references/json_output_structure.md.
Available Commands
-
search: Search cCREs by coordinates, accessions, or epigenetic signals.
uv run scripts/screen_api.py search \
--chromosome chr11 --start 5205263 --end 5207263 \
--output /tmp/search.json
-
nearby-genes: Find nearby genes for given cCRE accessions.
uv run scripts/screen_api.py nearby-genes \
EH38E1516972 --output /tmp/nearby.json
-
details: Get detailed information and biosample-specific max Z-scores for
a specific cCRE.
uv run scripts/screen_api.py details EH38E2941922 \
--output /tmp/details.json
-
biosamples: Get biosample metadata for an assembly.
uv run scripts/screen_api.py biosamples \
--output /tmp/biosamples.json
-
orthologs: Get orthologous cCREs in another assembly.
uv run scripts/screen_api.py orthologs EH38E2941922 \
--output /tmp/orthologs.json
-
linked-genes: Find linked genes via methods like HiC or eQTLs.
uv run scripts/screen_api.py linked-genes \
EH38E1516972 --output /tmp/linked.json
-
gene-expression: Get gene expression (TPM) across all biosamples for a
named gene. Internally resolves the gene symbol to an Ensembl gene ID, then
queries per-biosample RNA-seq quantifications.
uv run scripts/screen_api.py gene-expression GAPDH \
--output /tmp/gene_expr.json
-
entex: Get ENTEx data for a cCRE or genomic region.
uv run scripts/screen_api.py entex \
--accession EH38E1310345 \
--output /tmp/entex.json
uv run scripts/screen_api.py entex \
--region chr1:1000068:1000409 \
--output /tmp/entex.json
-
gwas: Query genome-wide association studies, SNPs, or enrichment data.
uv run scripts/screen_api.py gwas studies \
--output /tmp/gwas.json
uv run scripts/screen_api.py gwas snps --study \
Ahola-Olli_AV-27989323-Eotaxin_levels \
--output /tmp/gwas_snps.json
You can supply the --assembly mm10 or --assembly grch38 flag to explicitly
request a specific assembly for most commands. By default, the script targets
grch38 but will automatically fall back to mm10 if no results are found or
if the query fails.
ENCODE Portal REST API (Direct Access)
For accessing raw experiments, ChIP-seq peaks, or other datasets that are not
represented as cCREs in SCREEN, use the scripts/encode_portal_api.py script.
It allows custom queries to the ENCODE Portal REST API.
Usage
uv run scripts/encode_portal_api.py search "type=Experiment&target.label=ZNF549" --output /tmp/znf549_experiments.json
Data Analysis Tips
When analyzing .bed or .bigBed files downloaded from ENCODE, standard
bioinformatics tools are highly recommended for finding overlaps (e.g., between
gene promoters and peaks):
bedtools: For fast mathematical operations on genomic intervals.
bigBedToBed: For converting binary BigBed files to readable BED
format.
pybedtools: A Python wrapper for bedtools.
Write custom logic if these tools are not pre-installed.
Custom Queries (SCREEN GraphQL)
If you need to make a complex GraphQL query that the script does not support,
read references/graphql_schema.md for a reference of available queries,
arguments, and return fields in the SCREEN GraphQL API.