head file1.seqz
chromosome position base.ref depth.normal depth.tumor depth.ratio Af Bf zygosity.normal GC.percent good.reads AB.normal AB.tumor tumor.strand
chr1 13183 A 8 12 1.5 1.0 0 hom 56.0 1 A . 0
chr1 13184 G 8 12 1.5 1.0 0 hom 56.0 1 G . 0
chr1 13185 C 9 12 1.333 1.0 0 hom 56.0 1 C . 0
tail file1.seqz
chrM 16557 T 31 17 0.548 1.0 0 hom 33.3333333333 1 T . 0
chrM 16558 A 33 17 0.515 1.0 0 hom 33.3333333333 1 A . 0
chrM 16559 A 33 17 0.515 1.0 0 hom 33.3333333333 1 A . 0
zcat file1.pileup.gz | cut -f 1 | uniq
chr1
chr2
chr3
chr4
chr5
chr6
chr7
chr8
chr9
chr10
chr11
chr12
chr13
chr14
chr15
chr16
chr17
chr18
chr19
chr20
chr21
chr22
chrX
chrY
chrM
zcat file1.seqz.gz | cut -f 1 | uniq
chromosome
chr1
chr2
chr3
chr4
chr5
chr6
chr7
chr8
chr9
chr10
chr11
chr12
chr13
chr14
chr15
chr16
chr17
chr18
chr19
chr20
chr21
chr22
chrX
chrY
chrM
Would you happen to know why this is so?
Thanks,
Hima
Dear Hima,
Unfortunately chromosome M gives problems in the extraction step. Probably because of the lack of heterozygous positions.
I should implement a cleaner way to handle this situation in future versions.
Could you try to select the chromosomes to sequenza.extract in the argument "chromosome.list"? You can pass a vector of the chromosome you would like to extract, eg: paste0(" chr", c(1:22,"X","Y").
Best
Francesco
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Dear Hima,
Unfortunately chromosome M gives problems in the extraction step. Probably because of the lack of heterozygous positions.
I should implement a cleaner way to handle this situation in future versions.
Could you try to select the chromosomes to sequenza.extract in the argument "chromosome.list"? You can pass a vector of the chromosome you would like to extract, eg: paste0(" chr", c(1:22,"X","Y").
Best
Francesco
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