User Activity

  • Posted a comment on ticket #36 on popoolation2

    Is this issue already resolved? I am encountering the same problem

  • Modified a comment on ticket #37 on popoolation2

    I see that everyting is on the + strand, but 2 exon and 2 CDS sequences are on the - strand. So this might be causing the error. Any suggestions on how to resolve this issue? https://drive.google.com/open?id=1G8eQ-T_YBRavZRY9KIWER5Si7m58XmYo

  • Modified a comment on ticket #37 on popoolation2

    https://drive.google.com/open?id=1qczN_WFK3yurzZwbrxXDRuAyqCQ6sPwy

  • Modified a comment on ticket #37 on popoolation2
  • Modified a comment on ticket #37 on popoolation2

    https://drive.google.com/open?id=1qczN_WFK3yurzZwbrxXDRuAyqCQ6sPwy

  • Posted a comment on ticket #37 on popoolation2

    https://drive.google.com/open?id=1qczN_WFK3yurzZwbrxXDRuAyqCQ6sPwy

  • Created ticket #37 on popoolation2

    Problem creating genewise sync file

  • Posted a comment on ticket #32 on popoolation2

    Ok, so I tried making a new .sync file with "sanger" as quality encoding and now my .sync file is perfectly fine! FastQC was telling me that my files were encoded in illumina and I also used the Illumina HiSeq 4000 platform. At least my sync file is ok now without "null" and errors showing up when i calculate Fst.

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sadtrex
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