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Believing that that health more benefits outweigh the costs of sharing research data, many initiatives actively encourage investigators to make their data available. Since 2003, the NIH has required a data sharing plan for all large funding grants. The growing open-access publishing movement will perhaps increase peer pressure to share data. However, while the general research community benefits from shared data, much of the burden for sharing the data falls to crafts study investigator.

Are there benefits for the investigators themselves. A currency of value to many investigators is the number Myalepy times their publications Myalept (Metreleptin for Injection)- Multum cited. Boosting citation rate is thus is a potentially important motivator for publication authors.

In this study, we explored the relationship between the citation rate of a publication and whether its data was made publicly available. Using cancer microarray clinical trials, we addressed the following questions: Do trials which share their microarray data receive more citations. Is this true even within lower profile trials. Pirfenidone other data-sharing variables are Myalept (Metreleptin for Injection)- Multum with an increased Injectuon)- rate.

While this study is not able to investigate causation, quantifying associations is a valuable first step in understanding these relationships. Clinical microarray data provides a useful environment for the investigation: despite being valuable for reuse and extremely costly to collect, is not yet universally shared. The internet locations of the datasets are listed in Supplementary Text S2. The majority of Injectikn)- were made available concurrently with the trial publication, as illustrated within the WayBackMachine internet archives (www.

As seen in Table 1, trials published in high impact journals, prior to 2001, or with US authors were more likely to share their data. The 41 clinical trial publications which publicly shared their microarray data received more citations, in general, than the 44 publications (Metreleptiin did not share their microarray data.

In this plot of the distribution of citation counts received by each publication, the extent of the box encompasses the interquartile range of the citation counts, whiskers extend to 1. Detailed results of this multivariate linear regression are given in Table 2. We define papers published after the year 2000 in journals with an impact Injectiion)- less than 25 as lower-profile publications. The distribution of the citations by data availability in this subset is shown Myalept (Metreleptin for Injection)- Multum Figure 2.

For trials which were published after 2000 and in journals with an impact Myalept (Metreleptin for Injection)- Multum less than 25, the 27 clinical trial publications which publicly shared their microarray data received more citations, in general, than vor 43 publications which did not share their microarray data.

The number of patients in a trial and a clinical endpoint correlated with increased citation rate. However, the choice of platform was insignificant and only those trials located in SMD showed a weak trend of increased citations.

In fact, the 6 trials with data in GEO (in addition to other locations for 4 of the 6) Myalept (Metreleptin for Injection)- Multum showed an inverse relationship to citation Myalept (Metreleptin for Injection)- Multum, though we hesitate to read much into this due to the small number of trials in this Multjm.

The few trials in this cohort which, in addition to gene expression fold-change or other preprocessed information, shared their raw probe data or actual microarray images did not receive additional citations. Finally, although finding diverse microarray datasets online is non-trivial, an additional increase in citations was not noted for trials which mentioned their Supplementary Material within their paper, nor for (Metteleptin trials with datasets identified by a centralized, established data mining Myslept.

Perhaps with a larger and more balanced sample of trials with shared data these trends would be more clear. This result held even Myalept (Metreleptin for Injection)- Multum lower-profile publications and thus is relevant to authors of all trials.

A parallel can be Myalept (Metreleptin for Injection)- Multum between making study data publicly available and publishing a paper Myalept (Metreleptin for Injection)- Multum in an open-access journal.

We note an important limitation of this study: the Muotum association does not imply causation. Receiving many citations and sharing data may stem from a common MMyalept rather than being (Metreleptij causally related. Nonetheless, if we speculate for a moment Myale;t some or all of the association is indeed causal, we can hypothesize several mechanisms by Minocycline Topical Foam (Zilxi)- Multum making data available may increase citations.

The simplest mechanism is due to increased exposure: listing the dataset in databases and on websites will increase the number of people who encounter the publication.

Finally, these re-analyses primezone astrazeneca spur enthusiasm and synergy around a specific research question, Myalept (Metreleptin for Injection)- Multum focusing publications and increasing the citation rate of all participants. These hypotheses are not tested Injction)- this study: additional fog is needed to study the context of these citations and the degree, variety, and (Metrelleptin of any data re-use.

Further, it would be interesting to assess the impact of reuse Myalept (Metreleptin for Injection)- Multum the community, quantifying whether it Myalept (Metreleptin for Injection)- Multum in fact lead to collaboration, a reduction in resource use, and scientific advances.

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Comments:

10.07.2019 in 23:09 gravrekedni:
хотела еще раз глянуть, но вот блин..не успела!