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Download gene set libraries from Enrichr in GMT format for ssGSEA - done in parallel with async
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from pathlib import Path | |
import parmap | |
import requests | |
def update(gsll): | |
return [g for g in gsll if not (output_dir / (g + ".gmt")).exists()] | |
def get(gsl): | |
f = output_dir / (gsl + ".gmt") | |
if f.exists(): | |
return | |
with requests.get(url + gsl) as req: | |
if req.ok: | |
with open(f, "w") as h: | |
h.write(req.content.decode()) | |
output_dir = Path("gene_set_libraries") | |
output_dir.mkdir(exist_ok=True) | |
url = "https://maayanlab.cloud/Enrichr/geneSetLibrary?mode=text&libraryName=" | |
gsllf = "gsls.enrichr.txt" | |
gsll = update(open(gsllf, "r").read().strip().split("\n")) | |
while gsll: | |
req = parmap.map_async(get, gsll) | |
try: | |
res = req.get() | |
except requests.exceptions.ChunkedEncodingError: | |
pass | |
gsll = update(gsll) | |
# # To run in serial: | |
# for gsl in tqdm(gsll): | |
# get(gsl) |
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Genes_Associated_with_NIH_Grants | |
Cancer_Cell_Line_Encyclopedia | |
Achilles_fitness_decrease | |
Achilles_fitness_increase | |
Aging_Perturbations_from_GEO_down | |
Aging_Perturbations_from_GEO_up | |
Allen_Brain_Atlas_down | |
Allen_Brain_Atlas_up | |
ARCHS4_Cell-lines | |
ARCHS4_IDG_Coexp | |
ARCHS4_Kinases_Coexp | |
ARCHS4_TFs_Coexp | |
ARCHS4_Tissues | |
BioCarta_2013 | |
BioCarta_2015 | |
BioCarta_2016 | |
BioPlanet_2019 | |
BioPlex_2017 | |
CCLE_Proteomics_2020 | |
ChEA_2013 | |
ChEA_2015 | |
ChEA_2016 | |
Chromosome_Location | |
Chromosome_Location_hg19 | |
ClinVar_2019 | |
CORUM | |
COVID-19_Related_Gene_Sets | |
Data_Acquisition_Method_Most_Popular_Genes | |
dbGaP | |
DepMap_WG_CRISPR_Screens_Broad_CellLines_2019 | |
DepMap_WG_CRISPR_Screens_Sanger_CellLines_2019 | |
Disease_Perturbations_from_GEO_down | |
Disease_Perturbations_from_GEO_up | |
Disease_Signatures_from_GEO_down_2014 | |
Disease_Signatures_from_GEO_up_2014 | |
DisGeNET | |
Drug_Perturbations_from_GEO_2014 | |
Drug_Perturbations_from_GEO_down | |
Drug_Perturbations_from_GEO_up | |
DrugMatrix | |
DSigDB | |
Elsevier_Pathway_Collection | |
ENCODE_and_ChEA_Consensus_TFs_from_ChIP-X | |
ENCODE_Histone_Modifications_2013 | |
ENCODE_Histone_Modifications_2015 | |
ENCODE_TF_ChIP-seq_2014 | |
ENCODE_TF_ChIP-seq_2015 | |
Enrichr_Libraries_Most_Popular_Genes | |
Enrichr_Submissions_TF-Gene_Coocurrence | |
Enrichr_Users_Contributed_Lists_2020 | |
Epigenomics_Roadmap_HM_ChIP-seq | |
ESCAPE | |
Gene_Perturbations_from_GEO_down | |
Gene_Perturbations_from_GEO_up | |
GeneSigDB | |
Genome_Browser_PWMs | |
GO_Biological_Process_2013 | |
GO_Biological_Process_2015 | |
GO_Biological_Process_2017 | |
GO_Biological_Process_2017b | |
GO_Biological_Process_2018 | |
GO_Cellular_Component_2013 | |
GO_Cellular_Component_2015 | |
GO_Cellular_Component_2017 | |
GO_Cellular_Component_2017b | |
GO_Cellular_Component_2018 | |
GO_Molecular_Function_2013 | |
GO_Molecular_Function_2015 | |
GO_Molecular_Function_2017 | |
GO_Molecular_Function_2017b | |
GO_Molecular_Function_2018 | |
GTEx_Tissue_Sample_Gene_Expression_Profiles_down | |
GTEx_Tissue_Sample_Gene_Expression_Profiles_up | |
GWAS_Catalog_2019 | |
HMDB_Metabolites | |
HMS_LINCS_KinomeScan | |
HomoloGene | |
Human_Gene_Atlas | |
Human_Phenotype_Ontology | |
HumanCyc_2015 | |
HumanCyc_2016 | |
huMAP | |
InterPro_Domains_2019 | |
Jensen_COMPARTMENTS | |
Jensen_DISEASES | |
Jensen_TISSUES | |
KEA_2013 | |
KEA_2015 | |
KEGG_2013 | |
KEGG_2015 | |
KEGG_2016 | |
KEGG_2019_Human | |
KEGG_2019_Mouse | |
Kinase_Perturbations_from_GEO_down | |
Kinase_Perturbations_from_GEO_up | |
L1000_Kinase_and_GPCR_Perturbations_down | |
L1000_Kinase_and_GPCR_Perturbations_up | |
Ligand_Perturbations_from_GEO_down | |
Ligand_Perturbations_from_GEO_up | |
LINCS_L1000_Chem_Pert_down | |
LINCS_L1000_Chem_Pert_up | |
LINCS_L1000_Ligand_Perturbations_down | |
LINCS_L1000_Ligand_Perturbations_up | |
lncHUB_lncRNA_Co-Expression | |
MCF7_Perturbations_from_GEO_down | |
MCF7_Perturbations_from_GEO_up | |
MGI_Mammalian_Phenotype_2013 | |
MGI_Mammalian_Phenotype_2017 | |
MGI_Mammalian_Phenotype_Level_3 | |
MGI_Mammalian_Phenotype_Level_4 | |
MGI_Mammalian_Phenotype_Level_4_2019 | |
Microbe_Perturbations_from_GEO_down | |
Microbe_Perturbations_from_GEO_up | |
miRTarBase_2017 | |
Mouse_Gene_Atlas | |
MSigDB_Computational | |
MSigDB_Hallmark_2020 | |
MSigDB_Oncogenic_Signatures | |
NCI-60_Cancer_Cell_Lines | |
NCI-Nature_2015 | |
NCI-Nature_2016 | |
NIH_Funded_PIs_2017_AutoRIF_ARCHS4_Predictions | |
NIH_Funded_PIs_2017_GeneRIF_ARCHS4_Predictions | |
NIH_Funded_PIs_2017_Human_AutoRIF | |
NIH_Funded_PIs_2017_Human_GeneRIF | |
NURSA_Human_Endogenous_Complexome | |
Old_CMAP_down | |
Old_CMAP_up | |
OMIM_Disease | |
OMIM_Expanded | |
Panther_2015 | |
Panther_2016 | |
Pfam_Domains_2019 | |
Pfam_InterPro_Domains | |
PheWeb_2019 | |
Phosphatase_Substrates_from_DEPOD | |
PPI_Hub_Proteins | |
ProteomicsDB_2020 | |
Rare_Diseases_AutoRIF_ARCHS4_Predictions | |
Rare_Diseases_AutoRIF_Gene_Lists | |
Rare_Diseases_GeneRIF_ARCHS4_Predictions | |
Rare_Diseases_GeneRIF_Gene_Lists | |
Reactome_2013 | |
Reactome_2015 | |
Reactome_2016 | |
RNA-Seq_Disease_Gene_and_Drug_Signatures_from_GEO | |
SILAC_Phosphoproteomics | |
SubCell_BarCode | |
SysMyo_Muscle_Gene_Sets | |
Table_Mining_of_CRISPR_Studies | |
TargetScan_microRNA | |
TargetScan_microRNA_2017 | |
TF-LOF_Expression_from_GEO | |
TF_Perturbations_Followed_by_Expression | |
TG_GATES_2020 | |
Tissue_Protein_Expression_from_Human_Proteome_Map | |
Tissue_Protein_Expression_from_ProteomicsDB | |
Transcription_Factor_PPIs | |
TRANSFAC_and_JASPAR_PWMs | |
TRRUST_Transcription_Factors_2019 | |
UK_Biobank_GWAS_v1 | |
Virus-Host_PPI_P-HIPSTer_2020 | |
Virus_Perturbations_from_GEO_down | |
Virus_Perturbations_from_GEO_up | |
VirusMINT | |
WikiPathways_2013 | |
WikiPathways_2015 | |
WikiPathways_2016 | |
WikiPathways_2019_Human | |
WikiPathways_2019_Mouse |
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