Comments (2)
It seems lots of Alu insertions reported from your results (vcf file having ~8000 records?). This is abnormal. We would expect to have around ~1200 germline Alu insertions for each sample. Those "errors" seems ok for me, as we don't expect Alu transductions, thus we didn't check the flanking regions.
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Sorry for the confusion. 8000 is the size of the file, about 8000 bytes. And about 20 somatic Alu insertion in the output. And thank you very much, I think the outputs are reasonable and correct:)) Thank you again!
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Related Issues (20)
- interpretation of GENE_INFO in output file HOT 1
- Long read cannot find temp files HOT 1
- xTea Long_read SyntaxWarning HOT 6
- line 1133, IOError: [Errno 2] No such file or directory: 'null' HOT 1
- x_TEA_main.py: error: no such option: --bamsnap HOT 2
- Very long length of L1 insertion HOT 1
- Long_reads: File detailing which reads show transductions of deletions HOT 1
- temp files burst out HOT 2
- Possible to merge TE sites and do genotyping in each sample? HOT 1
- xTea_long getting stuck, no errors, during wtpoa-cns, running HG38 HOT 2
- xTea output file understanding HOT 5
- About the case-control analysis in Illumina Short-read WGS Data HOT 3
- filtering HOT 4
- Will the coverage of BAM files affect the xTea results? HOT 3
- Input file for pseudogene insertion calling HOT 1
- Issue with Somatic Insertion Genotyping in Case-Control Mode HOT 3
- what's the meaning of "REF_REP=Fall_in_Alu_copy_2.5"? HOT 1
- Cannot find the target directory: xTea/xtea/genotyping/trained_model_ssc_py2_random_forest_two_category.pkl. HOT 3
- xTea for assembled genomes HOT 1
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