Question: Keeping Aditional Data In The Aachanges Tool
0
Ximena Bonilla • 10 wrote:
Dear Galaxy staff,
I have recently started using your tool and it has been really
helpful,
thank you!
When using Human Genome Variation, aaChanges, I would like to keep
some
extra lines in the output file from either of the input files. In the
tool
description it says I should be able to keep them:
"...chromosome, start, and end position as well as the SNP. The SNP
can be
given using ambiguous-nucleotide symbols or a list of two to four
alleles
separated by '/'. *Any other columns in the first input file will not
be
used but will be kept for the output*. The second input file
contains..."
However, I haven't found a way of actually have them in the output
file.
What am I missing/doing incorrectly?
What I've been trying to keep by the way is rs IDs or Ensembl gene
IDs.
Thank you in advance for your answer.
Kind regards,
Ximena
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modified 7.5 years ago
by
Jennifer Hillman Jackson ♦ 25k
•
written
7.5 years ago by
Ximena Bonilla • 10