Interactive Biosoftware
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Interactive Biosoftware is the creator of the Alamut™ Software Suite, the original mutation interpretation software used by leading genetic researchers around the world.
Interactive Biosoftware is the creator of the Alamut™ Software Suite, the original mutation interpretation software used by leading genetic researchers around the world.
23 followers
Interactive Biosoftware's posts
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National Cancer Institute sequenced the exomes of 60 of its cancer cell lines, and cataloged the genetic variations, with the results available in public databases ... Cancer Genetic Variations Database Generated for Therapies http://bit.ly/14UEnDj #Science #Business #ScienceBusiness
Our #biosoftware #Alamut conveniently streamlines post- #sequencing analyses of detected variants & precisely catalogs mutations- Get your free 30-day trial now!
http://bit.ly/160m2G2t
http://bit.ly/160m2G2t
Our #biosoftware #Alamut conveniently streamlines post- #sequencing analyses of detected variants & precisely catalogs mutations- Get your free 30-day trial now!
http://bit.ly/160m2G2t
http://bit.ly/160m2G2t
Our #biosoftware #Alamut conveniently streamlines post- #sequencing analyses of detected variants & precisely catalogs mutations- Get your free 30-day trial now!
http://bit.ly/160m2G2t
http://bit.ly/160m2G2t
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Our #biosoftware #Alamut conveniently streamlines post- #sequencing analyses of detected variants & precisely catalogs mutations- Get your free 30-day trial now!
http://bit.ly/160m2G2t
http://bit.ly/160m2G2t
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Discover Alamut, our mutation interpretation software designed to help scientists interpret human genome variants. With more than 18,000 human protein coding genes, Alamut is a gene browser that offers advanced visualization of gene-related annotations.
These annotations are based on public data sources such as NCBI, UCSC, and EBI.
Beside data, Alamut integrates a number of prediction tools enabling fast and accurate variant interpretation and reporting. Users can easily manage and annotate mutations and create documented variant reports that comply with HGVS recommendations.
#bioinformatics #variantannotation #mutations #datavisualization
These annotations are based on public data sources such as NCBI, UCSC, and EBI.
Beside data, Alamut integrates a number of prediction tools enabling fast and accurate variant interpretation and reporting. Users can easily manage and annotate mutations and create documented variant reports that comply with HGVS recommendations.
#bioinformatics #variantannotation #mutations #datavisualization
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Discover Alamut, our mutation interpretation software designed to help scientists interpret human genome variants. With more than 18,000 human protein coding genes, Alamut is a gene browser that offers advanced visualization of gene-related annotations.
These annotations are based on public data sources such as NCBI, UCSC, and EBI.
Beside data, Alamut integrates a number of prediction tools enabling fast and accurate variant interpretation and reporting. Users can easily manage and annotate mutations and create documented variant reports that comply with HGVS recommendations.
#variantannotation #variant #genetics #mutations #bioinformatics
These annotations are based on public data sources such as NCBI, UCSC, and EBI.
Beside data, Alamut integrates a number of prediction tools enabling fast and accurate variant interpretation and reporting. Users can easily manage and annotate mutations and create documented variant reports that comply with HGVS recommendations.
#variantannotation #variant #genetics #mutations #bioinformatics
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"NGS clinical sequencing market will grow to more than $1.0 billion in 2015". #NGS #clinical #sequencing
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Looking forward to the 2013 ICCG International Collaboration for Clinical Genomics Meeting this Thursday. Visit us at booth #7!
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