I am following one paper https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-016-2486-8 in order to distinguish the core and accessory chromosomes of several genomes that I am working with. For this I did PROmer alignment, and generated the output files (delta and coords files). From the paper they say that the scaffolds with >=30% of their length covered by unique promer matches to core chromosomes of reference genome were considered core chromosomes and the rest as accessory chromosome.
The codes that I used are as below:
What I do not understand is how to calculate the coverage of each scaffold from this data and set the cutoffs as >=30% to define the core chromosomes. Please help!!
Thanks
AP
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Hello everyone,
I am following one paper https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-016-2486-8 in order to distinguish the core and accessory chromosomes of several genomes that I am working with. For this I did PROmer alignment, and generated the output files (delta and coords files). From the paper they say that the scaffolds with >=30% of their length covered by unique promer matches to core chromosomes of reference genome were considered core chromosomes and the rest as accessory chromosome.
The codes that I used are as below:
The output that I am getting now (coords file) looks like this:
What I do not understand is how to calculate the coverage of each scaffold from this data and set the cutoffs as >=30% to define the core chromosomes. Please help!!
Thanks
AP