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    <title>lukas on Sparks Lab</title>
    <link>/authors/lukas/</link>
    <description>Recent content in lukas on Sparks Lab</description>
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    <lastBuildDate>Sun, 13 Sep 2020 00:00:00 +0000</lastBuildDate>
    
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      <title>DDIG: Detecting DIsease-causing Genetic variations</title>
      <link>/server/ddig/</link>
      <pubDate>Sun, 13 Sep 2020 00:00:00 +0000</pubDate>
      
      <guid>/server/ddig/</guid>
      <description>DDIG currently supports prediction of protein-coding
non-frameshifting (NFS) indels,
frameshifting (FS) indels,
nonsense (protein-truncating) and
synonymous (same-sense, silent) variants in the GRCh37/hg19 assembly of the human genome.
 E-mail address (optional):    Target (optional):    Input your variants (format and examples):        
Check the Job Queue Status  

Publications:
Synonymous variants:
M. Livingstone, L. Folkman, Y. Yang, P.</description>
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      <title>EASE-MM: Prediction of mutation-induced stability changes</title>
      <link>/server/ease-mm/</link>
      <pubDate>Wed, 05 Feb 2020 00:00:00 +0000</pubDate>
      
      <guid>/server/ease-mm/</guid>
      <description>EASE-MM supports prediction of missense mutations
specified as amino acid substitutions (protein input)
or as nsSNV variants (genome input)
in the GRCh37/hg19 assembly of the human genome.

 E-mail address (optional):    Target (optional):    Input your sequence and mutations:    SEQ: my_short_seq RDSGTVWGALGHGINLNIPNFQMTDDIDEVRWERGSTLVAEFKRKMKPFLKSGAFEILANGDLKIKNLTRDDSGTYNVTVYSTNGTRILDKALDLRILE MUT: A40G L16V G4A     
Check the Job Queue Status  

Publication:</description>
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