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Written by Kim Gurwitz     April 01, 2016     768   0
"SPANR addresses a key unmet challenge in genomics research, which is to ascertain how single nucleotide variations (SNVs) cause splicing misregulation and may lead to disease. Unlike any other approach,...
 
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Written by JP Maree     March 09, 2016     244   0
BioWardrobe Experiment Management System, which allows users to store, visualize and analyze epigenomic and transcriptomic next-generation sequencing data using a biologist-friendly, web-based graphical user interface without the need for programming...
 
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Written by Kim Gurwitz     April 01, 2016     259   0
"Candidate genes prioritization through genomic data fusion" - from the Endeavour website
 
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Written by Kim Gurwitz     April 01, 2016     317   0
"eXtasy is a pipeline for ranking nonsynonymous single nucleotide variants given a specific phenotype" - from the eXtasy website.
 
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Written by Kim Gurwitz     April 15, 2016     254   0
'Genephony is an online tool for the manipulation of large datasets of genomic information. It can be used as a browser for genomic data, as a high-throughput annotation tool, and...
 
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Written by Kim Gurwitz     April 08, 2016     347   0
*Interpret next generation sequencing results *Identify & Prioritize genes and variants according to their relevance to diseases and phenotypes of interest *Explore relationships between genes and gene variants and selected...
 
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6 results - showing 1 - 6