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Thread | Thread Starter | Forum | Replies | Last Post |
Minimum Criteria to Publish ChIP-seq data | ETHANol | Epigenetics | 7 | 12-04-2011 05:35 AM |
Lets publish the Wiki! | dan | Wiki Discussion | 108 | 09-07-2011 10:10 AM |
SEQanswers mentioned for the second time in a major journal | ECO | Site Announcements | 3 | 08-01-2011 09:51 AM |
Jim Watson in Excruciating Detail: 454/Baylor Publish Complete Genome Sequence | ECO | Literature Watch | 1 | 04-16-2008 03:43 PM |
Welcome to SEQanswers.com! | ECO | Site Announcements | 0 | 10-28-2007 04:59 PM |
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#321 | |
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I think this will make a nice figure and some points for the discussion. Maybe we can get this data from ECO? Additionally, it would be nice to get the location data from the google analytics of this site. |
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#322 | |
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#323 | |
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Since I talked to the editor of GM November 23rd, we really should get something out to them soon if we end up going with their journal. |
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#324 | |
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Marco |
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#325 | |
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Marco |
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#326 |
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#327 |
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#328 |
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Robs, please check your email.
Anyone want to produce a figure from the stats?
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Marco Last edited by marcowanger; 12-01-2011 at 06:50 AM. |
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#329 |
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#330 | |
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Clearly, however, it can be demonstrated that one aspect of the forum's ongoing importance to the Wiki is the community's desire to maintain and support (a repository of) extensive and active discussion concerning tools cataloged at the forum's younger sister site, the SeqWiki. Now, there are many other aspects to the importance of the forum, SeqAnswers, which is why good editorial feedback suggested an article in it's own right. But any material taken pretty much directly from the published NAR article is not going to fly no matter how hard you spin it. |
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#331 |
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#332 |
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Thank you robs
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#333 |
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Hi Marco,
For the benefit of all the great contributers and contributions to this thread I am posting an editorial reply you have previously posted on the Wiki. "Genome Biology -inquiry by marcowanger, reply on 29th Nov 2011 Thank you for your email in which you offer to submit a Correspondence manuscript on the SEQanswers community to Genome Biology. I am very sorry about the delay in getting back to you about it. Having discussed and considered your proposal with my colleagues, I am afraid that we are unable to consider the manuscript you describe for publication. I'm sorry that we can't be more positive but we are sure you won't have any difficulties in publishing your article elsewhere. Thank you for your interest in Genome Biology." Also for the benefit of all contributers to this particular thread, I request that you disclose reviewer comments from the NAR Wiki article and post a copy of the initial August 16 2011 draft as well as the revised October 25, 2011 draft submitted by you , Dan, and ECO. Thanks. |
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#334 | |
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The reviewers' comment and our replies are disclosed in the wiki page (http://seqanswers.com/wiki/Publicati...AR_2012)/Reply) We discussed and replied with the writing exactly as described in the wiki. The initial draft is at here (http://seqanswers.com/wiki/Publication/Paper_(NAR_2012)) The revised MS (except the correction made on spelling and typos) is exactly as you can get in NAR website now. The corrections made on the 25th Oct 2011 version are deposited in (http://seqanswers.com/wiki/Publicati...2)/Corrections). Thanks for asking this. We have started disclosing everything from the initial idea, to drafting, to submission, answering reviewers' comment, and correction to production proof copy, everything on the SEQwiki page. ![]()
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Marco Last edited by marcowanger; 12-02-2011 at 01:25 AM. Reason: typo |
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#335 | ||
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#336 |
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I think we should move forward with Genome Medicine as our target journal. We should prepare a COMMENTARY article as the editor suggested. I will post the requirements again, shortly.
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#337 | |
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#338 |
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Points to focus on:
"Genome Medicine publishes open access research articles of outstanding quality and broad interest in all areas of medicine studied from a genomic or post-genomic perspective. The journal has a special focus on the latest technologies, including genomic methods, proteomics, bioinformatics and computational biology, and findings that have an impact on the understanding and management of human health and disease. Correspondence items discuss material published in Genome Medicine or issues of exceptional interest to the broad readership of the journal." 1. How does SEQanswers advance genomics and how does the board specifically enable the use or improvement of the latest genomic methods, bioinformatics methods, etc.? 2. Why would SEQanswers be of broad interest to the readership of Genome Medicine? In other words, how is this useful to bioinformatics, genome biologists, and clinical researchers. The BWA vs BOWTIE2 thread is a good example for bioinformatics. There are some good examples also for wet lab sequencing methods as well. To be relevant to human medicine, it does not mean we must discuss disease. There are lots of model systems that would be interesting. Also methods/discussions that concern population genetics are of CRITICAL value to clinicians understanding human patient groups. In addition for personal genomics, reducing FPs is a big issue. The larger the list of mutations, the less likely they will actionable. So really even the BWA vs. BOWTIE2 thread is relevant in medicine, as is discussions of dbSNP, etc. "Correspondence should be between 800-3000 words." I think we if take what we have, along with Rob's excellent figures; and then add a discussion of the above two points, we will have a nice correspondence that will probably be close to 1000-1500 words or so. No need to write anymore than is necessary especially if we are including those figures. We will also need an up to 200 word abstract. Obviously for a correspondence of 1500 words I do not think our abstract really has to be 200 words, but that is the reported maximum. |
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#339 |
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We received our feedback almost two weeks ago, so I would recommend we finalize the text and figures next week. I would be happy to work on the two points I suggested in the previous post. I think that we should quickly decide if we want a table/figure with the demographic data. Sounds like Rob will do this over the weekend.
We should also determine the final author list (sorted however everyone wants). I think Marco and Rob have taken a real lead on this manuscript but there are have been other contributors as well so we should identify and sort these authors. I am also going to start working on the final WORD/GDoc document that will contain a title, authors, keywords, abstract, etc. (all the sections and formatting we need) so that when the text is final, we can easily integrate it into the final document and submit. I think we have a great story and I think that getting this paper out to Genome Medicine will be good for the journal and also great for the SEQanswers community. Last edited by adaptivegenome; 12-02-2011 at 08:28 AM. Reason: typo |
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#340 |
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