The issue here is with chr4 status of homozygous deletion.
chr3 and chr8 display segments of heterozygous deletion (tcn, lcn)=(1,0) with different values of logR and logOR. If I understand this well, the difference is explained by the fact that the cellular fraction of both events is different, chr8 het del being more clonal than chr3 het del.
I guess that the interpretation here for chr4 is based on the same logic, meaning that chr4 homo del only happens in a very low proportion of tumour cells. But it seems to me that this region might also be merged to the normal (2,1) status even though there exists a non neglectable deviation from mean diploid logR level. What do you think ?
Extreme cases of this behaviour is when you have very noisy (wavy logR) data. In these cases you will observe over-segmentation of the data and applying a too low cval will end up in many (erroneous) short segments of homozygous deletion.
Considering all this, I wonder if you can elaborate a bit on the role of deltaCN parameter in preprocessing step and on how to use it. Using deltaCN=1 has given me quite good (pretty) results but I am not exactly sure about what I am doing here.
Thanks.
# packages versions (install from bioconda)
data.table_1.12.2 facets_0.5.14 pctGCdata_0.2.0
I would like to understand a behaviour that seems to occur quite often with facets.
Here I show an example taken from a WES paired samples analysis.
I have attached the final profile and here is an excerpt of
fit2$cncf
object (chr1 to chr8):The issue here is with chr4 status of homozygous deletion.
chr3 and chr8 display segments of heterozygous deletion (tcn, lcn)=(1,0) with different values of
logR
andlogOR
. If I understand this well, the difference is explained by the fact that the cellular fraction of both events is different, chr8 het del being more clonal than chr3 het del.I guess that the interpretation here for chr4 is based on the same logic, meaning that chr4 homo del only happens in a very low proportion of tumour cells. But it seems to me that this region might also be merged to the normal (2,1) status even though there exists a non neglectable deviation from mean diploid logR level. What do you think ?
Extreme cases of this behaviour is when you have very noisy (wavy logR) data. In these cases you will observe over-segmentation of the data and applying a too low cval will end up in many (erroneous) short segments of homozygous deletion.
Considering all this, I wonder if you can elaborate a bit on the role of
deltaCN
parameter in preprocessing step and on how to use it. UsingdeltaCN=1
has given me quite good (pretty) results but I am not exactly sure about what I am doing here.Thanks.