Hi Alain,
Sorry for the late reply,m I have just come back from a vocation.
I will change
vcf2bed.pl little late, which makes not convenient now…
i think the problem here is that you have not specified "-stand_emit_conf", by default, "-stand_emit_conf " is 30, so when you specify -stand_call_conf 1, it takes not effect, because it is less than the emit threshold. please just add an option that "-stand_emit_conf 0"
Thanks,
Yaping Liu
PhD candidate
in
USC Epigenome Center
University of Southern California
On Oct 20, 2012, at 7:23 PM, Alain Pacis wrote:
Dear Yaping Liu,
My name is Alain Pacis and I am Master's student in bioinformatics at University of Montreal with Dr. Barreiro.
I am currently working on the dendritic cell (DC) methylome to find changes in DNA methylation before and after infection to Myobacterium tuberculosis (MTB).
I started using BisSNP to get both the SNPs and methylation data from my bisulfite-treated sample aligned using Bismark (~10X coverage).
The problem is that the FILTER column for both snp.raw.vcf and cpg.raw.vcf output files doesn't indicate "PASS" and therefore vcf2bed.pl won't work unless that column indicates "PASS".
I even put the parameter stand_call_conf = 1 but it still did not work.
I used the following command:
java -Xmx48g -jar /RQusagers/pacisala/barreiro_group/ALAIN/BisSNP/BisSNP-0.73.jar -R /RQusagers/pacisala/barreiro_group/ALAIN/BisSNP/hg19_rCRSchrm.fa -T BisulfiteGenotyper -nt 12 -stand_call_conf 1 -I NEG81.adapt.fastq_bismark.sam_deduplicated.header.sorted.realigned.recal.bam -D /RQusagers/pacisala/barreiro_group/ALAIN/BisSNP/dbsnp_135.hg19.sort.sorted.again.vcf -vfn1 cpg.raw.vcf -vfn2 snp.raw.vcf