easy-entrez

Python REST API for Entrez E-Utilities, aiming to be easy to use and reliable.

Easy-entrez:

• makes common tasks easy thanks to simple Pythonic API,
• is typed and integrates well with mypy,
• is tested on Windows, Mac and Linux across Python 3.7, 3.8, 3.9 and 3.10,
• is limited in scope, allowing to focus on the reliability of the core code,
• does not use the stateful API as it is error-prone as seen on example of the alternative entrezpy.

Examples

from easy_entrez import EntrezAPI

entrez_api = EntrezAPI(
    'your-tool-name',
    'e@mail.com',
    # optional
    return_type='json'
)

# find up to 10 000 results for cancer in human
result = entrez_api.search('cancer AND human[organism]', max_results=10_000)

# data will be populated with JSON or XML (depending on the `return_type` value)
result.data

See more in the Demo notebook and documentation.

For a real-world example (i.e. used for this publication) see notebooks in multi-omics-state-of-the-field repository.

Fetching genes for a variant from dbSNP

Fetch the SNP record for rs6311:

rs6311 = entrez_api.fetch(['rs6311'], max_results=1, database='snp').data[0]
rs6311

Display the result:

from easy_entrez.parsing import xml_to_string

print(xml_to_string(rs6311))

Find the gene names for rs6311:

namespaces = {'ns0': 'https://www.ncbi.nlm.nih.gov/SNP/docsum'}
genes = [
    name.text
    for name in rs6311.findall('.//ns0:GENE_E/ns0:NAME', namespaces)
]
print(genes)

['HTR2A']

Fetch data for multiple variants at once:

result = entrez_api.fetch(['rs6311', 'rs662138'], max_results=10, database='snp')
gene_names = {
    'rs' + document_summary.get('uid'): [
        element.text
        for element in document_summary.findall('.//ns0:GENE_E/ns0:NAME', namespaces)
    ]
    for document_summary in result.data
}
print(gene_names)

{'rs6311': ['HTR2A'], 'rs662138': ['SLC22A1']}

Obtaining the chromosomal position from SNP rsID number

from pandas import DataFrame

result = entrez_api.fetch(['rs6311', 'rs662138'], max_results=10, database='snp')

variant_positions = DataFrame([
    {
        'id': 'rs' + document_summary.get('uid'),
        'chromosome': chromosome,
        'position': position
    }
    for document_summary in result.data
    for chrom_and_position in document_summary.findall('.//ns0:CHRPOS', namespaces)
    for chromosome, position in [chrom_and_position.text.split(':')]
])

variant_positions

	id	chromosome	position
0	rs6311	13	46897343
1	rs662138	6	160143444

Converting full variation/mutation data to tabular format

Parsing utilities can quickly extract the data to a VariantSet object holding pandas DataFrames with coordinates and alternative alleles frequencies:

from easy_entrez.parsing import parse_dbsnp_variants

variants = parse_dbsnp_variants(result)
variants

<VariantSet with 2 variants>

To get the coordinates:

variants.coordinates

rs_id	ref	alts	chrom	pos	chrom_prev	pos_prev	consequence
rs6311	C	A,T	13	46897343	13	47471478	upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
rs662138	C	G	6	160143444	6	160564476	intron_variant

For frequencies:

variants.alt_frequencies.head(5)  # using head to only display first 5 for brevity

	rs_id	allele	source_frequency	total_count	study	count
0	rs6311	T	0.44349	2221	1000Genomes	984.991
1	rs6311	T	0.411261	1585	ALSPAC	651.849
2	rs6311	T	0.331696	1486	Estonian	492.9
3	rs6311	T	0.35	14	GENOME_DK	4.9
4	rs6311	T	0.402529	56309	GnomAD	22666

Obtaining the SNP rs ID number from chromosomal position

You can use the query string directly:

results = entrez_api.search(
    '13[CHROMOSOME] AND human[ORGANISM] AND 31873085[POSITION]',
    database='snp',
    max_results=10
)
print(results.data['esearchresult']['idlist'])

['59296319', '17076752', '7336701', '4']

Or pass a dictionary (no validation of arguments is performed, AND conjunction is used):

results = entrez_api.search(
    dict(chromosome=13, organism='human', position=31873085),
    database='snp',
    max_results=10
)
print(results.data['esearchresult']['idlist'])

['59296319', '17076752', '7336701', '4']

The base position should use the latest genome assembly (GRCh38 at the time of writing); you can use the position in previous assembly coordinates by replacing POSITION with POSITION_GRCH37. For more information of the arguments accepted by the SNP database see the entrez help page on NCBI website.

Find PubMed ID from DOI

When searching GWAS catalog PMID is needed over DOI. You can covert one to the other using:

def doi_term(doi: str) -> str:
    """Prepare DOI for PubMed search"""
    doi = (
        doi
        .replace('http://', 'https://')
        .replace('https://doi.org/', '')
    )
    return f'"{doi}"[Publisher ID]'


result = entrez_api.search(
    doi_term('https://doi.org/10.3389/fcell.2021.626821'),
    database='pubmed',
    max_results=1
)
result.data['esearchresult']['idlist']

['33834021']

Installation

Requires Python 3.6+. Install with:

pip install easy-entrez

If you wish to enable (optional, tqdm-based) progress bars use:

pip install easy-entrez[with_progress_bars]

If you wish to enable (optional, pandas-based) parsing utilities use:

pip install easy-entrez[with_parsing_utils]

Alternatives

You might want to try:

• biopython.Entrez - biopython is a heavy dependency, but probably good choice if you already use it
• pubmedpy - provides interesting utilities for parsing the responses
• entrez - appears to have a comparable scope but quite different API
• entrezpy - this one did not work well for me (hence this package), but may have improved since