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Hello!
Thanks for developing and supporting PhylogicNDT.
I used PureCN (based on ABSOLUTE ideas to generate input for PhylogicNDT): https://bioconductor.org/packages/release/bioc/html/PureCN.html
Namely, I used this https://github.com/naumenko-sa/bioscripts/blob/master/phylogicndt/purecn2phylogicndt.R script to select columns for files with variants and segments. Also, I was using purity information from PureCN.
My samples.sif file:
sample_id maf_fn seg_fn purity timepoint s1 s1.maf.tsv s1.cn.tsv 0.89 1 s2 s2.maf.tsv s2.cn.tsv 0.68 1 s3 s3.maf.tsv s3.cn.tsv 0.94 1
maf_fn file format:
Hugo_Symbol Chromosome Start_position Reference_Allele Tumor_Seq_Allele2 t_ref_count t_alt_count local_cn_a1 local_cn_a2
seg_fn file format as in the example: https://github.com/broadinstitute/PhylogicNDT/blob/master/ExampleData/Simulations/Example_SegFile.txt
ID Chromosome Start_position End_Position A1_CN A2_CN
PhylogicNDT call (clustering and tree building):
PhylogicNDT.py \ Cluster \ -i project \ -sif samples.sif \ --maf_input_type calc_ccf \ -rb
I'm getting a parsing error:
File "/PhylogicNDT/data/Sample.py", line 478, in _resolve_CnEvents start = int(row['Start.bp'])
https://github.com/broadinstitute/PhylogicNDT/blob/master/data/Sample.py#L478
PhylogicNDT interprets it as alleliccapseg format which is different from what I've generated. How to force timing format for CN files?
alleliccapseg
timing
When running without CN files phylogic_report.html has been generated (but CNVs were not mapped).
Does anybody else have experience using PureCN output as input for PhylogicNDT?
Thanks! Sergey
The text was updated successfully, but these errors were encountered:
@naumenko-sa running through the same issue. Have you found a way to fix this?
Sorry, something went wrong.
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Hello!
Thanks for developing and supporting PhylogicNDT.
I used PureCN (based on ABSOLUTE ideas to generate input for PhylogicNDT):
https://bioconductor.org/packages/release/bioc/html/PureCN.html
Namely, I used this https://github.com/naumenko-sa/bioscripts/blob/master/phylogicndt/purecn2phylogicndt.R
script to select columns for files with variants and segments. Also, I was using purity information from PureCN.
My samples.sif file:
maf_fn file format:
seg_fn file format as in the example:
https://github.com/broadinstitute/PhylogicNDT/blob/master/ExampleData/Simulations/Example_SegFile.txt
PhylogicNDT call (clustering and tree building):
I'm getting a parsing error:
https://github.com/broadinstitute/PhylogicNDT/blob/master/data/Sample.py#L478
PhylogicNDT interprets it as
alleliccapseg
format which is different from what I've generated.How to force
timing
format for CN files?When running without CN files phylogic_report.html has been generated (but CNVs were not mapped).
Does anybody else have experience using PureCN output as input for PhylogicNDT?
Thanks!
Sergey
The text was updated successfully, but these errors were encountered: