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Thread | Thread Starter | Forum | Replies | Last Post |
Time to publish SEQanswers? | dan | Site Feedback/Suggestions | 430 | 03-16-2012 02:45 AM |
Minimum Criteria to Publish ChIP-seq data | ETHANol | Epigenetics | 7 | 12-04-2011 04:35 AM |
The SEQanswers wiki: a wiki database of tools for high-throughput sequencing analysis | marcowanger | Literature Watch | 5 | 11-15-2011 06:48 PM |
The SEQanswers wiki: a wiki database of tools for high-throughput sequencing analysis | marcowanger | Wiki Discussion | 1 | 11-15-2011 08:58 AM |
Jim Watson in Excruciating Detail: 454/Baylor Publish Complete Genome Sequence | ECO | Literature Watch | 1 | 04-16-2008 02:43 PM |
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#101 | |
wiki wiki
Location: Cambridge, England Join Date: Jul 2008
Posts: 267
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Ah, I see the citation count on findit now. Well... If you can build an API interface to a findit screen scraping script, I'd be happy to use that in SEQwiki. I'd need something like: http://some.box/findit.cgi?q=<PMID|TITLE> It could return JSON, XML or CSV, as described here: http://www.mediawiki.org/wiki/Extension:External_Data You could host it on the Google app server if you like python. Cheers, Dan. Last edited by dan; 08-16-2011 at 02:26 AM. Reason: Didn't look. |
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#102 |
Senior Member
Location: Hong Kong Join Date: Dec 2008
Posts: 350
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On the right panel, you see
More like this 258 Articles that cite this from Scopus 237 Articles that cite this from Web of Science®
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Marco |
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#103 |
Senior Member
Location: Boston Join Date: Feb 2008
Posts: 693
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It seems that FindIt does not hold the data. When FindIt displays a page, it queries WebOfScience (WOS) on the fly. WOS must provide an interface to get the data. Nonetheless, WOS is a paid site. I do not know if the interface is public.
Another citation resource you may consider is <http://www.ebi.ac.uk/citexplore/webservice.jsp> from EBI. Still WOS has a better coverage, though. PS: As I have just checked, CiteXplore also links to WOS, so there must be some way to query WOS. <example: http://www.ebi.ac.uk/citexplore/citationDetails.do?externalId=19451168&dataSource=MED&citedCount=1> |
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#104 |
Senior Member
Location: Hong Kong Join Date: Dec 2008
Posts: 350
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It seems you have to be licensed to use WOS api
http://bibwild.wordpress.com/2009/04...link-resolver/
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Marco |
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#105 |
Senior Member
Location: Boston Join Date: Feb 2008
Posts: 693
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Is it legitimate to get the WOS citation number from this CiteXplore link? It is just a plain HTML page, fairly easy to parse out.
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#106 | |
wiki wiki
Location: Cambridge, England Join Date: Jul 2008
Posts: 267
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This is the core idea behind the creation of the world wide web. I think people who try to protect data 'on the web' have forgotten what the web is. If you don't want it downloaded, don't put it on the web. Just my 2p. |
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#107 | |
Senior Member
Location: Hong Kong Join Date: Dec 2008
Posts: 350
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Dear Dan,
Quickly wrote something that fetch abstract and citation count based on PMID. May you modify it to fits your mediawiki? Let me know what I can help. p.s. Thanks Heng for the EBI's link. Regards, Marco Quote:
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Marco |
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#108 |
Senior Member
Location: Boston Join Date: Feb 2008
Posts: 693
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I am a little concerned about the list of "most popular tools" at the front page of wiki. I think it is hard to find the right criteria about what should go into the list. For example, should we include EMBOSS suite, BLAST, FASTA, BioPerl/BioPython and CAP3? CAP3 should certainly go to the list. We may still use BLAST/FASTA to map reads in highly diverged regions (at least I use BLAST occasionally). I know people are using EMBOSS to convert formats. BioPerl/BioPython are certainly widely used. These tools all have at least a couple of thousands of citations and will immediately take the top few places in the list.
On the other hand, the citations for the Erange and ChIPSeq software are counted based on the papers describing the biotechnology rather than on the methods. I cite the two papers when I refer to chip-seq and rna-seq in general. But I do not cite them for the methods. The ChIPSeq software is rarely used so far as I know (the link is broken now). Erange is still widely used, but I am not sure if it is the most popular any more. The most accurate measurement of popularity of a tool is the number of citations for using the tool to process sequencing data. For some papers (e.g. maq/bowtie), all citations are like this. But for some other papers (e.g. BLAT/MUMmer/erange/chipseq), we can hardly know the answer. If we do not have solid criteria about what should be included in the frontpage, my opinion is to drop the list. Showing misleading data might be worse than showing nothing. Perhaps giving the timeline of each publication may be helpful in some aspects, but I guess it is very difficult to get this information and does not really solve all the problems. Anyway, whatever decision you made, I really appreciate all your efforts. Collecting citations is a hard thing. Last edited by lh3; 09-07-2011 at 08:37 AM. |
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