On the Galaxy web interface, the option to map sequences with Bowtie for Illumina reads is listed under the Tools heading "NGS: Mapping".
"Will you select a reference genome from your history or use a built-in index?" is the first question at the top of the web page. The options are: "Use a built-in index" or "Use one from the history".
If I have a genome index that is not available on the "built-in" list, can I upload this index file to Galaxy under the Get Data page and then select it under "Use one from the history"?
The index file is 3 GB, so any advice is appreciated before I try to upload it.
Thanks,
jjw
"Will you select a reference genome from your history or use a built-in index?" is the first question at the top of the web page. The options are: "Use a built-in index" or "Use one from the history".
If I have a genome index that is not available on the "built-in" list, can I upload this index file to Galaxy under the Get Data page and then select it under "Use one from the history"?
The index file is 3 GB, so any advice is appreciated before I try to upload it.
Thanks,
jjw