I am working with 454 single-end long-read data for a region on chr6, using hg19 and dbSNP build 135 as references. GATK Unifiedgenotyper with the option -glm INDEL returns no calls on realigned+recalibrated bam file and on recalibrated bam file. Using additional arguments, such as --output_mode EMIT_ALL_SITES, or setting call/emit thresholds, does not make a difference, either.
Earlier posts on this forum (http://seqanswers.com/forums/showthread.php?t=15634) indicate that a high sequencing error rate may be the cause.
So I wonder:
1. If resetting the sequencing error rate is the solution, how do I do it? Is this error rate reported in the bam file?
2. Are there other ways of tweaking GATK to deal with this problem?
Thanks for your help!
Earlier posts on this forum (http://seqanswers.com/forums/showthread.php?t=15634) indicate that a high sequencing error rate may be the cause.
So I wonder:
1. If resetting the sequencing error rate is the solution, how do I do it? Is this error rate reported in the bam file?
2. Are there other ways of tweaking GATK to deal with this problem?
Thanks for your help!
Comment