DataONE:Protocols/Find GEO reuses
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collect data on the of datasets in the published literature. This focuses on reuses of gene expression microarray datasets stored in NCBI's Gene Expression Omnibus (GEO) repository and tracks reuses attributed through accession numbers .
Revision as of 14:37, 15 July 2010
Identify reuses of GEO datasets
The aim of this protocol is to collect data on the reuses of datasets in the published literature. This particular protocol focuses on reuses of gene expression microarray datasets stored in NCBI's Gene Expression Omnibus (GEO) repository and tracks reuses attributed through accession numbers within the full text of articles in PubMed Central.
Little research has been done on the patterns and prevalence of data reuse. A few superstar success stories need no analysis: Data from Genbank and the Protein Data Bank are reused, heavily, successfully. They have generated important science that would not have been possible otherwise.
They are so successful, though, that people discount them as special cases.
So what does the reuse behaviour look like for other datasets?
We don’t know. It is difficult to track reuse. There have been a few surveys, but they suffer from limited scope and self-reporting biases. I gather that download stats are poorly correlated with perceived value. So let’s track reuse in the published literature.
- Query GEO for all GDS and GDS accession numbers for datasets
- Query PubMed Central for these accession numbers in the full text of PMC papers published between 1900 and 2009
- Enumerate the PMC papers that reused GEO data
- Estimate what percent of these papers depended on the GEO data for their scientific contribution
Used python source code:
NOTE: I'm still getting my git together, so the code at the above links may not be fully standalone or easily run by others. I'm working on it... in the meantime, feel free to email me if you want details!
Accession number formats
- look at both GSE and GDS accession numbers
- use both the raw ID number like 200007572 and the stripped version without the 200... prefix. For example, search for both 200007572 and 7572
- search for both accession number right beside the prefix, and with one space in between, so "GSE 7572" and "GSE7572"
Exclude data creation studies
- spot-check to make sure accession number is in the context of reuse... looks like there may be a few mentions in the context of depost in which the article is not tagged with pmc_gds[filter] (example: PMCID 2396644)
- do this for all the PMC article hits? looks like there are a few missing the filter, and it matters because it would erroneously inflate our reuse estimate
- could use query from my BioLink paper:
(geo OR omnibus) AND microarray AND "gene expression" AND accession NOT (databases OR user OR users OR (public AND accessed) OR (downloaded AND published))
- or the more simple:
"gene expression omnibus” AND (submitted OR deposited)
- to do this transparently, query PMC results for each of these words:
- to do this transparently, query PMC results for each of these words:
Estimate what percentage of reusers weren't the original authors
- see if AND pubmed_gds and NOT pmc_gds have any author overlaps? (note AND should be pubmed!)
- other idea: institution comparison using medline info
- better than submitter, because submitter not the whole story
- better than institution, because institution not precise in submission
Is the PMC paper by the same investigators as those who originally created the data?
- first pass: automatedly extracted a column that contained the last names at the intersection of the PMC reuse paper and those in the original data-creation paper and those in the GEO submission list
- if there was a lot of author overlap, coded it as a "CREATOR REUSE" paper
- also automatedly extracted the institution of the PMC reuse paper and the original data-creation paper. If there was overlap and some evidence of author overlap, coded it a "CREATOR REUSE" paper
- if there was no overlap in author or institution, coded it as NOT a "CREATOR REUSE" paper
- for ambiguous cases were there was an author in common between the two papers but it was a common name or the corresponding author addresses were different, I manually examined the PMC reuse paper and the data-creation paper to determine whether the common authors had the same initials and institutions. If yes, I coded it as a "CREATOR REUSE" paper, otherwise I coded it as NOT a "CREATIVE REUSE" paper
Extrapolate from PubMed Central to PubMed
- use "gene expression profiling"[mesh] query in PMC vs PubMed over time period in question to get relevant estimate
- restrict from 2007 to 2009
number of articles in PMC: 6311, number of articles in PubMed: 21569, so PMC contains 29.26% of related papers
- so we should multiply our number of scientific papers by about 3 to get estimate for all of scientific publishing
- To Do: compare results to GEO's list of 3rd party reuses: http://www.ncbi.nlm.nih.gov/projects/geo/info/ucitations.html
Extracted this raw data, one row for every (GEO accession number:PMCID of paper that includes the accession number) pair:
- is the PMC paper actually about data sharing into GEO rather than data reuse?
- is the PMC paper by the same investigators as those who originally created the data?
- if reuse, is it in the context of developing a method or tool?
- could use this data to see how many publications use any one dataset
- could use this data to look at average elapsed time between data submission and reuse, but only have short time period to consider... better off with data deposited longer ago
- can't use this particular data to see how many datasets each publication uses, because only looking at datasets from a given year
- A first snapshot of this data is included in a manuscript-in-progress
- What else on OpenWetWare links to this page
Assumptions, Limitations, and Unknowns
This protocol captures a subset of all dataset reuses because of several limitations:
- Many data citations are attributed without using accession numbers
- don't have a good way to estimate this yet
- would require a manual inventory, similar to Sarah's data citation inventory in DataONE summer 2010 project
- Many papers are not in PubMed Central
- we can estimate what percentage are and then try to extrapolate to all papers. For example, using "gene expression profiling"[mesh] query in PMC vs PubMed over 2007-2009 suggests PMC contains 30% of all related papers in PubMed
- many datasets will continue to be used in the future... these reuses are obviously not continued in our estimate
- our methods do not find studies that both create and reuse data
- to narrow down our query results, we automatedly eliminate studies that create data... even though these same studies may also reuse data
- we don't have an estimate of how many this is, would require manual inventory
- Doesn't capture reuse outside the peer-reviewed literature (for example, reuse during training)
Furthermore, extrapolations based on this data may be biased:
- Papers in PubMed Central may not be representative
- Deposits into PMC not stable over time, distribution may change over time, may be skewed based on open-access uptake or NIH-funding levels in various communities
- our estimates do not consider reuses after our study timeframe
- How to efficiently estimate what percent of these papers depended on the GEO data for their scientific contribution?
- Use Author-ity clusters to disambiguate authors
- Torvik VI and Smalheiser NR. . pmid:20072710.
- Keep track of GDS and GSE overlaps
- Piwowar, HA. Studying Reuse Of GEO Datasets In The Published Literature. Research Remix. July 5 2010. blog post
- Piwowar HA and Chapman WW. . pmid:18998887.
- Piwowar, Wendy W Chapman (2008) Linking database submissions to primary citations with PubMed Central. BioLINK 2008, Toronto Canada. Full text
Please feel free to post comments, questions, or improvements to this protocol. Happy to have your input! Please sign your name to your note by adding '''*~~~~''': to the beginning of your tip.
- List troubleshooting tips here.
- Anecdotal observations that might be of use to others can also be posted here.