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Submit Task - SPANR

SPANR Splicing-based Analysis of Variants. 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, this tool can analyze synonymous, missense and nonsense exonic SNVs, as well as intronic SNVs that are up to 300nt from splice junctions. If you use this tool in research, please cite. How the tool works. Context, the tool examines DNA sequences from the exon, it...

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Submit Task - SPANR | tools.genes.toronto.edu Reviews
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SPANR Splicing-based Analysis of Variants. 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, this tool can analyze synonymous, missense and nonsense exonic SNVs, as well as intronic SNVs that are up to 300nt from splice junctions. If you use this tool in research, please cite. How the tool works. Context, the tool examines DNA sequences from the exon, it...
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1 spanr alpha
2 about and contact
3 new task
4 try spidex
5 to learn more
6 context dependence
7 runtime
8 input format
9 delimited entries
10 the chromosome
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spanr alpha,about and contact,new task,try spidex,to learn more,context dependence,runtime,input format,delimited entries,the chromosome,chrom,1 offset,the reference allele,a/c/g/t,both,may be,var n,examples,separated,lynch syndrome examples,smn examples
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Submit Task - SPANR | tools.genes.toronto.edu Reviews

https://tools.genes.toronto.edu

SPANR Splicing-based Analysis of Variants. 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, this tool can analyze synonymous, missense and nonsense exonic SNVs, as well as intronic SNVs that are up to 300nt from splice junctions. If you use this tool in research, please cite. How the tool works. Context, the tool examines DNA sequences from the exon, it...

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everything-will-happen.com everything-will-happen.com

Generative Products | Everything Will Happen

http://www.everything-will-happen.com/posts/generative-products.html

It wasn’t until recently that machine learning moved from medical labs ( Spanr, genomics analysis. And search algorithms enhancement. Google’s recent acquisition of Deep Mind. IBM’s push of Watson. And other viral developments. Signal a looming shift into consumer products. As machine learning will be making its way into consumer hands there is going to be a need for design thinking to lead the way in shaping products for the consumer market. Deployment of a powerful codebase that can generate a set of v...

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Submit Task - SPANR

SPANR Splicing-based Analysis of Variants. 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, this tool can analyze synonymous, missense and nonsense exonic SNVs, as well as intronic SNVs that are up to 300nt from splice junctions. If you use this tool in research, please cite. How the tool works. Context, the tool examines DNA sequences from the exon, it...

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