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suggestions for manual #19

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kuhlwilm opened this issue Feb 13, 2023 · 0 comments
Open

suggestions for manual #19

kuhlwilm opened this issue Feb 13, 2023 · 0 comments
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documentation Improvements or additions to documentation

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@kuhlwilm
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Some (not urgent) suggestions for the manual

Overview

  • the variant is bi-allelic in reference and target population (source population is only annotated)

score

  • Typo: ^"dervied"
  • add the following on the vcf file: "The genotypes in the VCF file need to be segregating in the combined target and source population, and not contain non-variable sites across these individuals. If more individuals are included (such as potential source individuals), sites only variable in these should not be included.
  • add to the last section a description of each flag that can be provided (missing: match/mismatch flags)

quantile

  • ^"quanitles", ^"simualted"
  • "The target and reference sizes need to match the number of chromosomes in the real data to be analyzed."
  • "The index numbers of source and target populations are defined by the order of their appearance in the demes file."
  • (the rest is fine to refer to -h)
  • "In order to simulate a range of recombination rates, the sstar quantile function needs to be performed in replicates with the recombination rate steps, and the output tables need to be merged."

threshold

  • ^"determing"
  • When specifying a recombination map, simulations with sstar quantile need to be performed in recombination rate steps.
  • The option "--k" only plays a role depending on the number of recombination steps in the simulations, if I understood correctly. So, that should be mentioned...

matchrate

  • ^"specifiy"
  • last sentence is a fragment
  • So I understood correctly that there is no haplotype differentiation at the moment, right? If using phased data, it is treated the same way as unphased data; and a perfectly matching heterozygous segment would have a matchrate of 50%? Maybe we can discuss modifications for future versions (non-urgent).

tract

  • maybe mention the --diff flag
  • may be good to explain: "If two possible source genomes are provided, two separate files will be written, with the segments matching one of these two source genomes."
@xin-huang xin-huang self-assigned this Feb 14, 2023
@xin-huang xin-huang added the documentation Improvements or additions to documentation label May 24, 2023
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