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Thanks for a great tool! I am trying to use test_ctDNA on bam files from targeted panel sequencing data and with BAM files aligned to RefSeq: NCBI GRCH37 Reference Sequence. Even after changing the seqname style of the BSgenome.Hsapiens.UCSC.hg19 from UCSC to NCBI, I kept getting the error: "Error: Chromosomes in bam file don't match the specified reference".
I saw that the culprit chromosomes were these unlocalized sequences GL00* when I ran the get_bam_chr() function. These sequences failed to map in BSgenome when I switched from UCSC to NCBI.
Is there a way to skip the chromosomes in the BAM file that do not match the reference? Could that be added as a parameter to the test_ctDNA function?
Hi,
Thanks for a great tool! I am trying to use test_ctDNA on bam files from targeted panel sequencing data and with BAM files aligned to RefSeq: NCBI GRCH37 Reference Sequence. Even after changing the seqname style of the BSgenome.Hsapiens.UCSC.hg19 from UCSC to NCBI, I kept getting the error: "Error: Chromosomes in bam file don't match the specified reference".
I saw that the culprit chromosomes were these unlocalized sequences GL00* when I ran the get_bam_chr() function. These sequences failed to map in BSgenome when I switched from UCSC to NCBI.
Is there a way to skip the chromosomes in the BAM file that do not match the reference? Could that be added as a parameter to the test_ctDNA function?
Below is the code and the sessionInfo():
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