Closed beginner984 closed 4 years ago
This would not be possible because they are cohort specific.
But, If you want to show differences in mutation load you can use tmb
> par(mfrow = c(1, 2))
> tmb(maf = maf1)
> tmb(maf = maf2)
Sorry, given two maf objects what you mean by tab
> par(mfrow = c(1, 2))
> tmb(maf = maf1)
Error in tmb(maf = maf1) : could not find function "tmb"
You mean oncoplot?
You will have to update the package for this function.
Excuse me @PoisonAlien, by
tmb(maf = laml,captureSize = 50,logScale = FALSE)
I see Median : 1.84/mb, does this mean that 1.84 per each 50 mega bases of the genome
because captureSize = 50
?
When I put captureSize = 1
, I get this
Because I am working on a cancer for which a reference paper has been published in which says median was 6.4 such mutations per mega base
, that is why I worry I may I calculate TMB wrong that I see TMB as 1.84
Capture size indicates the size of genome that is sequenced. For example exome-seq with Agilent sureselect kit captures ~50mb of the genome. If you observe 100 mutations then your TMB is 100/50 = 2per mb. Probably there are more fancier ways to estimate TMB but here its just a simple division with capture size.
Sorry @PoisonAlien
I have to groups of patients for them I plotted mutational burden like this
My boss says I should find a way to make Y axis at the same scale I mean by bared eyes we can see the differences, for example looking at y axis one group crosses the 0 while another one is 0.5
Is there any possible change to the function can to this?
No its not possible.
Sorry @PoisonAlien
Total mutation burden in my samples is like
> tmb
Tumor_Sample_Barcode total total_perMB total_perMB_log
1: LP6008202-DNA_B03 7 0.14 -0.853871964
2: LP6008460-DNA_F02 49 0.98 -0.008773924
3: s59 55 1.10 0.041392685
I did not figure out what is the difference of total
and total_perMB
For instance for LP6008202-DNA_B03
total
is 7
but by mafSummary
, ms$variant.classification.summary
total
is 4395
Please you may help me of these definitions
Thank you
Can you post the below output?
getSampleSummary(ms)[Tumor_Sample_Barcode %in% c("LP6008202-DNA_B03", "LP6008460-DNA_F02", "s59")]
total
is the number of variants (excluding CNVs, and syn mutations) in a sample.
Thank you
> getSampleSummary(ms)[Tumor_Sample_Barcode %in% c("LP6008202-DNA_B03", "LP6008460-DNA_F02", "s59")]
Tumor_Sample_Barcode Frame_Shift_Del Frame_Shift_Ins In_Frame_Del In_Frame_Ins
1: s59 1 2 2 0
2: LP6008460-DNA_F02 1 1 1 1
3: LP6008202-DNA_B03 0 0 0 0
Missense_Mutation Nonsense_Mutation Nonstop_Mutation Splice_Site total
1: 48 2 0 0 55
2: 39 3 1 2 49
3: 7 0 0 0 7
>
>
Seems ok to me.
Hello @PoisonAlien
I have two groups
Is there any way to show mutation per sample with the scale? I thought in combining two groups by showing barcode but I noticed patients are placed irregularly regardless of their own groups.