Comments (4)
Is this for tumor-only or tumor-normal? Is freebayes designed for somatic variants?
from somaticseq.
Hi,
once again, thanks for the prompt reply!
I am using freebayes with tumor-normal matched samples. It seems that it should work for somatic variants.
My question is more general, though. I was wondering whether there was an "easy" way to use other callers.
I am just putting together a pipeline and can certainly use what somaticseq is designed for.
Thanks
Gianfilippo
from somaticseq.
I can add a feature to allow any new customized callers to be included in the near future. Before we complete and test that feature, however........
Right now, for the callers that are "officially supported," SomaticSeq may handle each of them differently, some are a bit more complicated than others, some are for legacy reasons. For MuTect2, for instance, it actually grabs some VCF information as training feature, and also look for both SOMATIC and PASS tag to be classified as a "+1" call.
For LoFreq and Platypus, they're a lot simpler. A call labeled PASS is considered a "+1" call. I'm not familiar with freebayes. If it follows the same label as LoFreq (i.e., PASS calls are considered somatic calls), you may try to pretend that it's LoFreq or Platypus VCF, and feed the freebayes VCF file as --lofreq-snv freebayes_snv_calls.vcf --lofreq-indel freebayes_indel_calls.vcf
or --platypus-vcf freebayes_snv_indel_calls.vcf
.
from somaticseq.
thanks. I can definitely try that and look forward to the new feature
from somaticseq.
Related Issues (20)
- Special setting for b37? HOT 14
- Question about simulating somatic mutations HOT 7
- Pretrained Classifier HOT 3
- Docker issue with latest version HOT 1
- SEQC2: Some high confidence SNVs and INDELs in VCF are outside of regions defined by High-Confidence_Regions_v1.2.bed HOT 2
- Somaticseq makeSomaticScripts.py running and output issues HOT 8
- Slow RNA variant calling HOT 8
- Question for the paper on establishing the reference call set HOT 3
- Where are the 10x Genomics single-cell copy number variation (CNV) analysis results? HOT 7
- Ground Truths required for training HOT 1
- somaticseq failing for same command it had previously successfully run HOT 11
- Applying internal filters to outputs before running SomaticSeq HOT 1
- Dockerized alignment workflow does not work with multiple input files HOT 5
- Error when running makeSomaticScripts with multiple threads HOT 3
- Output allele of the normal sample HOT 2
- UnboundLocalError: cannot access local variable 'normal_name' where it is not associated with a value HOT 10
- how to obtain all variants where the "FILTER" column is not labeled as "PASS" HOT 1
- Are multi-nucleotide and complex variants ignored? HOT 2
- Error when running FFPE training data from SEQ2C HOT 5
- AI consensus calling error on WGS samples HOT 9
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from somaticseq.