I made a new BWA file, this time using the hg19(full) genome. However, when I am trying to use DepthOfCoverage, the reference genomr is stucked on the hg_g1k_v37 (this is the only option to select), and I cannot change it to hg19(full). Most probably, because I selected hg_g1k_v37 in the previous time I tried to use DepthOfCoverage.
It seems as a bug? How can I change it?
The problem with this analysis probably has to do with a mismatch
between the genomes: the intervals obtained from UCSC (hg19) and the
BAM from your BWA (hg_g1k_v37) run.
UCSC does not contain the genome 'hg_g1k_v37' - the genome available
from UCSC is 'hg19'.
Even though these are technically the same human release, on a
practical level, they have a different arrangement for some of the
chromosomes. You can compare NBCI
GRCh37 with UCSC hg19
for an explanation.
Reference genomes must be exact in order to be used with
tools - base for base. When they are exact, the identifier will be
exact between Galaxy and the source (UCSC, Ensembl) or the full
Build name will provide enough information to make a connection to
NCBI or other.
Sometimes genomes are similar enough that a dataset sourced from one
can be used with another, if the database attribute is changed and
the data from the regions that differ is removed. This may be
possible in your case, only trying will let you know how difficult
it actually is with your analysis. The GATK pipeline is very
sensitive to exact inputs. You will need to be careful with genome
database assignments, etc. Following the links on the tool forms to
the GATK help pages can provide some more detail about expected
inputs, if this is something that you are going to try.
Good luck with the re-run!
Jen
Galaxy team
On 6/18/12 4:42 AM, Lilach Friedman wrote:
Hi,
I am trying to used Depth of Coverage to see the coverages is
specific intervals.
The intervals were taken from UCSC (exons of 2 genes), loaded
to Galaxy and the file type was changed to intervals.
I gave to Depth of Coverage two BAM files (resulted from BWA,
selection of only raws with the Matching pattern: XT:A:U, and
then SAM-to-BAM)
and the intervals file (in advanced GATK options).
The consensus genome is hg_g1k_v37.
I got the following error message:
An error
occurred running this job: Picked up _JAVA_OPTIONS:
-Djava.io.tmpdir=/space/g2main ##### ERROR
------------------------------------------------------------------------------------------ ##### ERROR A USER ERROR
has occurred (version 1.4-18-g80a4ce0): ##### ERROR The invalid
argume
Is it a bug, or did I do anything wrong?
I will be grateful for any help.
Thanks!
Lilach
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