Hi Daniel,
Thanks for your kind attention and advice.
I have followed the following workflow: I aligned my query sequences to
the reference genome using Bowtie; the Bowtie aligned SAM file was
subjected to filter-SAM before converting it to BAM. I have re-BAM-to-SAM
converted the BAM-file before subjecting it to pileup.
However, now I do have the Input format file (after pileup of SAM) but am
unable to convert it to BAM format to be able to submit it ti SICER.
Please see if you can suggest how to convert the Input files back to BAM.
I have tried changing directly through edit-attributes, but it shows
error.
AP
Hi AP,
SICER requires BED formatted input with at least 6 columns (for strand
information). You can convert your BAM files into SAM and then into
interval and BED format. Once you have your input in the BED (6+) format,
you should be able to use these tools. Please let us know if we can
provide additional information.
Thanks for using Galaxy,
Dan
On Nov 23, 2011, at 12:26 PM, Anupam Paliwal wrote:
Hi,
I want to use SICER or Find Peaks for peak calling on GALAXY.
I am using my aligned ChIP-seq tag .BAM files. However for both the
tools
the history is unable to pick the Bowtie-ligned SAM to BAM converted
files.
On the other hand, using MACS the same files are working nicely for peak
calling.
Thanks,
AP
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