Gene Ontology (GO)#
Pathways represent interconnected molecular networks of signaling cascades that govern critical cellular processes. They provide understandings cellular behavior mechanisms, insights of disease progression and treatment responses. In an R&D organization, managing pathways across different datasets are crucial for gaining insights of potential therapeutic targets and intervention strategies.
In this notebook we manage a pathway registry based on “2023 GO Biological Process” ontology. We’ll walk you through the steps of registering pathways and link them to genes.
In the following Standardize metadata on-the-fly notebook, we’ll demonstrate how to perform a pathway enrichment analysis and track the dataset with LaminDB.
Setup#
Warning
Please ensure that you have created or loaded a LaminDB instance before running the remaining part of this notebook!
This notebook follows the [CellTypist], which populate the CellType registry.
!lamin init --storage ./use-cases-registries --schema bionty
Show code cell output
✅ saved: User(uid='DzTjkKse', handle='testuser1', name='Test User1', updated_at=2024-01-31 09:59:19 UTC)
✅ saved: Storage(uid='jB3m7Ims', root='/home/runner/work/lamin-usecases/lamin-usecases/docs/use-cases-registries', type='local', updated_at=2024-01-31 09:59:19 UTC, created_by_id=1)
💡 loaded instance: testuser1/use-cases-registries
💡 did not register local instance on lamin.ai
import lamindb as ln
import bionty as bt
import gseapy as gp
bt.settings.organism = "human" # globally set organism
💡 lamindb instance: testuser1/use-cases-registries
2024-01-31 09:59:22,172:INFO - Failed to extract font properties from /usr/share/fonts/truetype/noto/NotoColorEmoji.ttf: In FT2Font: Can not load face (unknown file format; error code 0x2)
2024-01-31 09:59:22,185:INFO - generated new fontManager
Fetch GO pathways annotated with human genes using Enrichr#
First we fetch the “GO_Biological_Process_2023” pathways for humans using GSEApy which wraps GSEA and Enrichr.
go_bp = gp.get_library(name="GO_Biological_Process_2023", organism="Human")
print(f"Number of pathways {len(go_bp)}")
2024-01-31 09:59:23,464:INFO - Downloading and generating Enrichr library gene sets...
2024-01-31 09:59:29,503:INFO - 0001 gene_sets have been filtered out when max_size=2000 and min_size=0
Number of pathways 5406
go_bp["ATF6-mediated Unfolded Protein Response (GO:0036500)"]
['MBTPS1', 'MBTPS2', 'XBP1', 'ATF6B', 'DDIT3', 'CREBZF']
Parse out the ontology_id from keys, convert into the format of {ontology_id: (name, genes)}
def parse_ontology_id_from_keys(key):
"""Parse out the ontology id.
"ATF6-mediated Unfolded Protein Response (GO:0036500)" -> ("GO:0036500", "ATF6-mediated Unfolded Protein Response")
"""
id = key.split(" ")[-1].replace("(", "").replace(")", "")
name = key.replace(f" ({id})", "")
return (id, name)
go_bp_parsed = {}
for key, genes in go_bp.items():
id, name = parse_ontology_id_from_keys(key)
go_bp_parsed[id] = (name, genes)
go_bp_parsed["GO:0036500"]
('ATF6-mediated Unfolded Protein Response',
['MBTPS1', 'MBTPS2', 'XBP1', 'ATF6B', 'DDIT3', 'CREBZF'])
Register pathway ontology in LaminDB#
bionty = bt.Pathway.public()
bionty
PublicOntology
Entity: Pathway
Organism: all
Source: go, 2023-05-10
#terms: 47514
📖 .df(): ontology reference table
🔎 .lookup(): autocompletion of terms
🎯 .search(): free text search of terms
✅ .validate(): strictly validate values
🧐 .inspect(): full inspection of values
👽 .standardize(): convert to standardized names
🪜 .diff(): difference between two versions
🔗 .to_pronto(): Pronto.Ontology object
Next, we register all the pathways and genes in LaminDB to finally link pathways to genes.
Register pathway terms#
To register the pathways we make use of .from_values
to directly parse the annotated GO pathway ontology IDs into LaminDB.
pathway_records = bt.Pathway.from_values(go_bp_parsed.keys(), bt.Pathway.ontology_id)
bt.Pathway.from_public(ontology_id="GO:0015868")
Pathway(uid='5bQIT2QT', name='purine ribonucleotide transport', ontology_id='GO:0015868', description='The Directed Movement Of A Purine Ribonucleotide, Any Compound Consisting Of A Purine Ribonucleoside (A Purine Organic Base Attached To A Ribose Sugar) Esterified With (Ortho)Phosphate, Into, Out Of Or Within A Cell.', public_source_id=47, created_by_id=1)
ln.save(pathway_records, parents=False) # not recursing through parents
Register gene symbols#
Similarly, we use .from_values
for all Pathway associated genes to register them with LaminDB.
all_genes = {g for genes in go_bp.values() for g in genes}
gene_records = bt.Gene.from_values(all_genes, bt.Gene.symbol)
Show code cell output
❗ ambiguous validation in Bionty for 1082 records: 'CCDC40', 'DYRK1B', 'LHX1', 'NELFE', 'THEMIS', 'DHRS4L2', 'HLA-E', 'B3GALT4', 'OR2J1', 'ATP5IF1', 'GBAP1', 'SLC25A12', 'EPHA1', 'EEF2K', 'KIR2DS3', 'PTEN', 'TFPT', 'IL9R', 'WDR45', 'CCL23', ...
❗ did not create Gene records for 37 non-validated symbols: 'AFD1', 'AZF1', 'CCL4L1', 'DGS2', 'DUX3', 'DUX5', 'FOXL3-OT1', 'IGL', 'LOC100653049', 'LOC102723475', 'LOC102723996', 'LOC102724159', 'LOC107984156', 'LOC112268384', 'LOC122319436', 'LOC122513141', 'LOC122539214', 'LOC344967', 'MDRV', 'MTRNR2L1', ...
gene_records[:3]
[Gene(uid='rO4xYou1DPxv', symbol='NUMBL', ensembl_gene_id='ENSG00000105245', ncbi_gene_ids='9253', biotype='protein_coding', description='NUMB like endocytic adaptor protein ', synonyms='NUMB-R|NUMBLIKE|TNRC23|CAG3A|CTG3A|NUMBR', organism_id=1, public_source_id=9, created_by_id=1),
Gene(uid='7eHOdxO8ZruV', symbol='MID1', ensembl_gene_id='ENSG00000101871', ncbi_gene_ids='4281', biotype='protein_coding', description='midline 1 ', synonyms='RNF59|FXY|OS|TRIM18', organism_id=1, public_source_id=9, created_by_id=1),
Gene(uid='5cpWPrzoClVX', symbol='MYH10', ensembl_gene_id='ENSG00000133026', ncbi_gene_ids='4628', biotype='protein_coding', description='myosin heavy chain 10 ', synonyms='NMMHCB', organism_id=1, public_source_id=9, created_by_id=1)]
ln.save(gene_records);
Link pathway to genes#
Now that we are tracking all pathways and genes records, we can link both of them to make the pathways even more queryable.
gene_records_ids = {record.symbol: record for record in gene_records}
for pathway_record in pathway_records:
pathway_genes = go_bp_parsed.get(pathway_record.ontology_id)[1]
pathway_genes_records = [gene_records_ids.get(gene) for gene in pathway_genes]
pathway_record.genes.set(pathway_genes_records)
Now genes are linked to pathways:
pathway_record.genes.list("symbol")
['CAST', 'CARD8', 'CARD18', 'XIAP', 'CST7']
Move on to the next analysis: Standardize metadata on-the-fly