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annoPipeline - an API-enabled gene annotation pipeline

annoPipeline uses APIs from mygene.info and Entrez esummary to annotate a user-provided list of gene symbols.

Generates a pandas DataFrame with gene symbol, gene name, EntrezID, and bibliographic info for up to 5 pubmed publications where a functional reference was provided (more about functional references at GeneRIF).

Designed to be useful for tasks such as:

  • identifying relevant publications for a given function
  • analyzing publications trends for genes belonging to a common pathway
  • identifying influential PIs for a given gene network.

Reqirements:

  • Written for use with Python 3.7, not tested on other versions.

  • annoPipeline requires:

    • numpy >= 1.16.2
    • pandas >= 0.24.2
    • Biopython >= 1.73
    • openpyxl >= 2.6.1
    • requests >= 2.21.0

To Install:

pip install annoPipeline

Or clone the repo from github. Then, in the annoPipeline directory, run:

python setup.py install

Required dependencies will be installed if missing, may take a few seconds.

Example usage:

Execute the full annotation pipeline on a list of gene symbols like this:

import annoPipeline as ap

# define a list of genes you would like annotated
geneList = ['CDK2', 'FGFR1', 'SLC6A4']

# annoPipeline will execute full annotation pipeline (see individual functions below). 
df = ap.annoPipeline(geneList) # returns pandas df with annotations for gene and bibliographic info.
  • ap.annoPipeline will default save annotation output to Excel file named by geneList symbols separated by '_'.

Warning!

If querying a single gene, still pass as a list. For example:

import annoPipeline as ap

df = ap.annoPipeline(['CDK2']) # for single gene queries still include [] - will be fixed in later version

v0.0.1 Functionality

Task 1:

  1. From the MyGeneInfo API, use the “Gene query service" GET method to return details on a given list of human gene symbols.
  2. From the returned json, parse out the “name", “symbol" and “entrezgene" values and print to screen

Use queryGenes():

import annoPipeline as ap

geneList = ['CDK2', 'FGFR1', 'SLC6A4']

l1 = ap.queryGenes(geneList) # returns list of dicts where keys are default mygene fields (symbol,name,taxid,entrezgene,ensemblgene)

Task 2:

  1. Using the appropriate identifier from the above result, send a query to the MyGeneInfo “Gene annotation services" method for each gene
  2. From the resulting json, collate up to 5 generif descriptions per gene
  3. Write the results to an Excel spreadsheet with columns: gene_symbol, gene_name, entrez_id, generifs

Use getAnno():

import annoPipeline as ap

geneList = ['CDK2', 'FGFR1', 'SLC6A4']
l1 = ap.queryGenes(geneList)
l2 = ap.getAnno(l1, saveExcel=True) # saveExcel defaults False
  • returns pandas df with genes and up to 5 generifs from mygene.info.
  • default saveExcel=False, to save output to Excel must state True
  • if True, Excel file will be named by geneList symbols separated by '_'.

Task 3:

  1. Use the Pubmed IDs associated with the above generif content to extract additional bibliographic information.

Use addBibs():

import annoPipeline as ap

geneList = ['CDK2', 'FGFR1', 'SLC6A4']
l1 = ap.queryGenes(geneList)
l2 = ap.getAnno(l1)
l3 = ap.addBibs(l2) # will return df with genes and up to 5 generifs from mygene.info
  • Currently returns the following bibliographic information when available:
    • PubDate
    • Source
    • Title
    • LastAuthor
    • DOI
    • PmcRefCount

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