Hi everyone,
I ran variant calling using Manta (the SV caller) with both my tumor and normal BAM files. I checked the results in somaticSV.vcf.gz. How should I interpret these results (particularly the PR:SR)? Did Manta produce output that only shows the differences between the normal and tumor BAM files, or is it related to the reference genome?
Here’s an example of the rows I got:
#CHROM POS ID REF ALT QUAL FILTER INFO FORMAT TUMOR _SAMPLE NORMAL_SAMPLE
chr1 6032123 MantaDEL:535:0:1:0:0:0 T <DEL> . PASS END=6065447;SVTYPE=DEL;SVLEN=-33324;CIPOS=0,2;CIEND=0,2;HOMLEN=2;HOMSEQ=GC;SOMATIC;SOMATICSCORE=130 PR:SR 60,0:92,0 46,17:59,21*
If you have any recommendations for other tools to use for detecting large structural variants, please let me know
Thank you in advance.
Thank you :)
I've read on github I’m not sure how to make sense of this part:
FORMAT TUMOR _SAMPLE NORMAL_SAMPLE
PR:SR 60,0:92,0 46,17:59,21*
What is considered a good SOMATICSCORE in this context?
Ah, to that I have sadly no idea (I haven't really used Manta much before). There seems to be some additional information on how they score the somatic variants (which I'm guessing is
SOMATICSCORE) in the supplementary zip file on their publication (here). It should be in the file namedmanta_supplementary_text.pdf.