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can't find known selective sweeps #40
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One possible reason is that you are using a very wide window (1000). You
can try values in the range 12 to 50 for the window width (-w).
…On Thu, Aug 11, 2022 at 3:38 PM jdaron ***@***.***> wrote:
Dear
I have been using recently raisd in addition to other statistic
descriptive to look at pattern of positive selection in one of my
population.
Using pi, tajima's D and H12 I could strong signal of selection near
previously identified insecticide resistance genes such as cyp6p, Vgsc,
Gaba and Gste. However, when I used stats computed by raisd, patterns of
selection are not that clear anymore.
I was wondering if such difference could be due to a poor usage of the
tools. As input file I used a phased and polarized VCF file using the
following command line: RAiSD -n mypop -I myVCF.vcf -M 0 -y 2 -f -D -R -S
mypop.ids.lst -w 1000
Thanks for your answer,
Josquin
[image: LBVwil 1pop stats 10kbw]
<https://user-images.githubusercontent.com/9592106/184137397-7480df1d-d2e6-4ccb-9879-2068856c7d7c.png>
[image: LBVwil raisd 100]
<https://user-images.githubusercontent.com/9592106/184146390-3a816493-d2b8-436c-a78e-94e90ab0ed04.png>
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Nikolaos Alachiotis
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Hi Nikos, Thanks for your quick answer, here is another look at the plot using -w 50. As you can see, reducing the window size improved the detection of the sweep at the Gste and a bit Gaba loci. However I couldn't spot a signal at the cyp6p locus, which is potentially a soft sweep. On aspect of the plot bellow that makes me a bit worry is that the size of the pic for the mu stat at the Gste and Gaba loc, which is a bit little, especially compared to the pic observed with the H12 stat, which is also confirmed using xpehh stat. Do you know if I could make other adjustment to improve the performance of the program. For example I was wondering whether having heterogeneous SNP density would affect the performance of the program. |
Hi Josquin,
RAiSD is designed to detect hard sweeps, so not getting any signal in a
region where a soft sweep potentially is is expected.
As far as I can tell from the plots, the sfs signal is weaker than the
other two at the Gaba loc and maybe stronger at the Gste loc. Considering
that the sfs-stat in RAiSD looks at the singletons and N-1 class (N is the
sample size) only, you could either change the SNP classes included in the
calculation (-c) or assign a lower/higher weight to sfs per chromosome
(supported in version 3.1: https://github.com/pephco/raisd, see the help
menu options -VAREXP , -SFSEXP , -LDEXP ) .
Best regards,
Nikos A.
…On Wed, Aug 17, 2022 at 4:14 PM jdaron ***@***.***> wrote:
Hi Nikos, Thanks for your quick answer, here is another look at the plot
using -w 50. As you can see, reducing the window size improved the
detection of the sweep at the Gste and a bit Gaba loci. However I couldn't
spot a signal at the cyp6p locus, which is potentially a soft sweep.
On aspect of the plot bellow that makes me a bit worry is that the size of
the pic for the mu stat at the Gste and Gaba loc, which is a bit little,
especially compared to the pic observed with the H12 stat, which is also
confirmed using xpehh stat.
Do you know if I could make other adjustment to improve the performance of
the program. For example I was wondering whether having heterogeneous SNP
density would affect the performance of the program.
Thanks,
Josquin
[image: LBVwil raisd 50]
<https://user-images.githubusercontent.com/9592106/185153703-442bfe50-caf0-4771-b664-4e591cc24237.png>
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Nikolaos Alachiotis
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Dear
I have been using recently raisd in addition to other statistic descriptive to look at pattern of positive selection in one of my population.
Using pi, tajima's D and H12 I could strong signal of selection near previously identified insecticide resistance genes such as cyp6p, Vgsc, Gaba and Gste. However, when I used stats computed by raisd, patterns of selection are not that clear anymore.
I was wondering if such difference could be due to a poor usage of the tools. As input file I used a phased and polarized VCF file using the following command line: RAiSD -n mypop -I myVCF.vcf -M 0 -y 2 -f -D -R -S mypop.ids.lst -w 1000
Thanks for your answer,
Josquin
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