Closed nickjhathaway closed 7 years ago
Hi Nick.
Try to specify the region. I noticed in your bam file that you only have coverage at the very end of the reference. I managed to start it with this command line (replace with your file name)
amplian.py -b EBNA3cN1MIDJijoye-d1-EBV-1.sorted.bam -r ebv0:86264-86674 -f your_reference.fasta
Nevertheless, it seems that you have all reads in the same orientation, and this will make all detected SNVs invalid. You will find no SNVs in SNVs_0.010000_final.csv
, but they are listed in raw_snv.txt
. Your sample seems quite heterogeneous, though.
Please keep in mind that the different modes are described in this page.
Best. Osvaldo
Apologies, I had read the part of the local mode finding the area with the highest diversity and I thought it would take into account only regions that had coverage. Since I only have one region I thought it would find this automatically.
-Nick
Sorry quick question, is the region supplied 1-based or 0-based?
Nick
Discovery mode must be triggered with the appropriate flag. Barring mistakes, we follow samtools convention for region specification.
When running amplian.py I get the following error and I'm not sure what is causing it.
I'm running the following command
And I have put all my files including output from amplian.py here, http://bib8.umassmed.edu/~hathawan/shorah/
Any help would be appreciated, thanks!
Nick