<![CDATA[BOL: Related items]]> https://bioinformaticsonline.com/related/41146?offset=460 https://bioinformaticsonline.com/bookmarks/view/12963/cosmos-our-workflow-management-system-for-ngs-data Wed, 23 Jul 2014 07:29:14 -0500 https://bioinformaticsonline.com/bookmarks/view/12963/cosmos-our-workflow-management-system-for-ngs-data <![CDATA[COSMOS, our workflow management system for NGS data]]> COSMOS, our Python-based management system for implementing large-scale parallel workflows focusing on, but not restricted to, large-scale short-read "NGS" sequencing data is open-access published via Advance Access in Bioinformatics (Gafni et al. 2014).  It is also available for download for non-commercial academic and research purposes at:

 http://cosmos.hms.harvard.edu/.

Address of the bookmark: https://cosmos.hms.harvard.edu/

]]> Jit https://bioinformaticsonline.com/researchlabs/view/17652/arraygen-bioinformatics-genomics-group Sun, 28 Sep 2014 14:09:55 -0500 <![CDATA[ArrayGen Bioinformatics Genomics Group]]> ArrayGen is a global bioinformatics company which is a one stop solution for microarray designing and genomics data analysis. Our novel Array Design Approach Strategy (ADAS) aims to condense the time lag between demands of scientific community and manufacture industry, thereby expediting research processes.

ArrayGen specializes in Genomics data analysis and research, as we believe in the level of precision, predictability, benchmark-ability, and data analysis capability of genomics data over other forms of biological data. ArrayGen constantly strives to develop new solutions, and plug the existing gaps in the technological advancement of the field.

More http://www.arraygen.com/

]]> https://bioinformaticsonline.com/news/view/18741/a-powerful-yet-simple-gene-set-analysis-tool-for-interpreting-rna-seq-and-ngs-results Thu, 30 Oct 2014 09:19:29 -0500 https://bioinformaticsonline.com/news/view/18741/a-powerful-yet-simple-gene-set-analysis-tool-for-interpreting-rna-seq-and-ngs-results <![CDATA[A powerful, yet simple, gene set analysis tool for interpreting RNA-seq and NGS results.]]> LifeMap Sciences is introducing GeneAnalytics, our new gene set analysis tool, which is applicable for NGS results and differentially expressed gene lists from variable sources. GeneAnalytics provides gene associations with tissues & cells, diseases, pathways, GO terms and compounds.

Our main advantages over other similar tools are:

  • GeneAnalytics is very simple and intuitive to use.
  • GeneAnalytics is based on our proprietary databases – GeneCards, MalaCards, PathCards and LifeMap Discovery, each of them integrates information from a very large number of resources.
  • GeneAnalytics supplies links for extensive background information on each of the matched results.

 

I invite you to try it out for free at geneanalytics.genecards.org, and would be happy to hear your comments and thoughts on how we can improve.

 

Yours,

Shani Ben-Ari Fuchs

LifeMap Sciences Team

]]> Shani https://bioinformaticsonline.com/bookmarks/view/19631/rosalind-bioinformatics-problems Thu, 18 Dec 2014 10:32:48 -0600 https://bioinformaticsonline.com/bookmarks/view/19631/rosalind-bioinformatics-problems <![CDATA[Rosalind Bioinformatics problems !!!]]> Rosalind is a platform for learning bioinformatics and programming through problem solving. Take a tour to get the hang of how Rosalind works.

http://rosalind.info/problems/list-view/

Address of the bookmark: http://rosalind.info/problems/list-view/

]]> Abhi