Closed Martaprf closed 2 years ago
Hi, were you processing another sample at the same time that also had the sample name of SAMPLE1
? could you remove the teste
directory and start the process again?
Hi,
Yes I am trying with two samples at the same time, but they don´t have the name of SAMPLE1, maybe I need some argument two put the samples names!!!!
can you show the read-groups from both the bams that you are running at once?
Ok, I allredy see the problem, my read-groups have the same SM for the two samples, so maybe I need put there the id of samples?
samtools view -H 10.postprocessed.bam | grep @RG @RG ID:10 SM:SAMPLE1 PL:ILLUMINA LB:10.ATGAGGCC+CAATTAAC PU:HTGNKDSXY.2 samtools view -H 11.postprocessed.bam | grep @RG @RG ID:11 SM:SAMPLE1 PL:ILLUMINA LB:11.ACTAAGAT+CCGCGGTT PU:HTGNKDSXY.2
Thanks a lot for the help!
Great. Thanks for following up.
Helllo,
I have been using smoove for a while, but now I got a error message that I do not understand:
My command line is :
/home/mferreira/programs/smoove-0.2.8/smoove call -x --name sample_10 --fasta /home/mferreira/WGS_RM/reference_genome/Homo_sapiens.GRCh38.dna_sm.primary_assembly.fa -p 10 --outdir teste --genotype /home/mferreira/WGS_RM/alignments/post_processed/others/10.postprocessed.bam
Someone can help me to understand what I am made wrong?
Thanks Marta