Dear all,
Just a brief message to point you also to GenomeQuest's new beta offering in NGS sequence data management and analysis. I think the offering is pretty exciting and may be valuable for researchers and bioinformaticists. For you to decide...
You can try it for free with no obligation: www.genomequest.com. It runs in your web browser.
Currently we support RNA-Seq, Variant calling, Rapid Annotation (metagenomics), and long read assembly, as well as high-throughput mapping. CHiP-Seq, micro RNA, other assembly tools, and much more will be rolled out shortly. All of the world's reference data is kept up to date inside the system so you get up-to-the-minute accuracy. And you can upload and use your own reference data if you prefer. Of course, there are APIs for bioinformaticists to extend and integrate the system, and we're about to release a huge update to the APIs that make it stronger still. Again, much much more to come in the coming weeks and months. I'll let it speak for itself.
Most importantly, we're looking for your detailed help to make it better. We have a linkedin group for feature requests athttp://www.linkedin.com/groups?gid=2056733 and I'd welcome any comments you have directly via email, as well.
Thanks for letting me have the opportunity to announce the new product.
Best regards,
Richard
[email protected]
Just a brief message to point you also to GenomeQuest's new beta offering in NGS sequence data management and analysis. I think the offering is pretty exciting and may be valuable for researchers and bioinformaticists. For you to decide...
You can try it for free with no obligation: www.genomequest.com. It runs in your web browser.
Currently we support RNA-Seq, Variant calling, Rapid Annotation (metagenomics), and long read assembly, as well as high-throughput mapping. CHiP-Seq, micro RNA, other assembly tools, and much more will be rolled out shortly. All of the world's reference data is kept up to date inside the system so you get up-to-the-minute accuracy. And you can upload and use your own reference data if you prefer. Of course, there are APIs for bioinformaticists to extend and integrate the system, and we're about to release a huge update to the APIs that make it stronger still. Again, much much more to come in the coming weeks and months. I'll let it speak for itself.
Most importantly, we're looking for your detailed help to make it better. We have a linkedin group for feature requests athttp://www.linkedin.com/groups?gid=2056733 and I'd welcome any comments you have directly via email, as well.
Thanks for letting me have the opportunity to announce the new product.
Best regards,
Richard
[email protected]
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