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Automated validation of genetic variants from large databases: ensuring that variant references refer to the same genomic locations

Some initial comparisons of HGMD & OMIM, nice to incl. ClinVar in the future

http://bioinformatics.oxfordjournals.org/content/27/6/891

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This entry was posted on Sunday, April 26th, 2015 at 9:45 am and is filed under SciLit, Uncategorized. You can follow any responses to this entry through the RSS 2.0 feed. Responses are currently closed, but you can trackback from your own site.

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