Comments (5)
from genomescope.
Thank you so much for the prompt reply. Yes, this belongs to Listeria Monocytogenes.
a) if I got you correct you came up with those numbers [(98% unique (2%
repetitive) and with very low heterozygosity)], based on the genome haploid length which is 3032448 bp. Next in order to see a repetitive content percentage, we divide 34907 / 3032448 bp which is approx 2% and while the unique one is 2997541/3032448 = approx 98%. Am I correct here ?????
b) The plot which we get here : Genome scope profile. The only difference which I can see in both of them is the second one has coverage threshold? what is the significance, and usage of these two plots, how are they different? Moreover, these two plot gives these number [ dup: 1.59%, unique: 98.8 %, kcov: 17.4, error:1.1%] what does kcov imply, The mean of these plots are even different. how can we say that the plot is giving correct value, how are plot interpreted?
c) The genome scope can be used to analyze repeat content for a larger eukaryotic genome size even like humans for example. Just that we will need to adjust the kmer number based on it. Am I right??
Thanks for the help. I really appreciate it.
from genomescope.
from genomescope.
Thanks for responding back, I wanted to confirm one more thing, I want to use the Genome Scope approach in order to see the percentage of repetitive elements in a genus of beetle, which has a genome size close to the human being. In that scenario should I use a range of kmers size, and see by using which size of kmer will give me minimum error rate, and choose that particular kmer value to interpret the repetitive content of the genome. ???? This is just a thought because I read somewhere for a larger genome, it good change kmer size.
Is there any place where I can read about the plots generated by the genome_scope?? Lastly from the genome_Scope, we do not come to about the different types of repetitive element percentages in the genome, right??
I am sorry for the trouble and thanks a lot for the help.
from genomescope.
from genomescope.
Related Issues (20)
- Low model fit while ran Genomescope 2.0
- Strange genomescope result HOT 1
- High heterozygous? HOT 3
- No file upload message HOT 1
- Unable to converge HOT 3
- 503 Service Unavailable HOT 2
- mergeing HiFi data of two samples didn't increase hetorozygosity
- Heterozygosity rate < 0 HOT 3
- expectations for pooled samples HOT 2
- Heterozygous tetraploid genome model fit HOT 2
- GenomeScope Output from PacBio Hifi ccs Reads is Confounding HOT 3
- Model and observations don't converge HOT 3
- dup (in figure) and bias (in model.txt) HOT 2
- Follow up RE: Confounding GenomeScope Output HOT 5
- Ploidy determination HOT 1
- Heterozygous peak identified as errors? HOT 3
- Estimated genome size is half HOT 2
- Should a larger K value be chosen? HOT 1
- Is command line for ploidy different? HOT 4
- Please help me to understand output
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from genomescope.