3.2. Nucleic and peptide kmer and nullpeptide detection

IM Ioannis Mouratidis
FB Fotis A. Baltoumas
NC Nikol Chantzi
MP Michail Patsakis
CC Candace S.Y. Chan
AM Austin Montgomery
MK Maxwell A. Konnaris
EA Eleni Aplakidou
GG George C. Georgakopoulos
AD Anshuman Das
DC Dionysios V. Chartoumpekis
JK Jasna Kovac
GP Georgios A. Pavlopoulos
IG Ilias Georgakopoulos-Soares
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The identification of kmers was performed following previously established definitions defined in [18]. Nullomer and nullpeptide detection were performed as previously described in [18] for each species at each kmer length.

Identification of nucleic and peptide quasi-primes.

DNA quasi-prime identification was performed by identifying kmers that were present in each reference genome and nullomers in every other reference genome. Similarly, peptide quasi-prime identification was performed by identifying kmers that were present in each reference proteome and nullomers in every other reference proteome.

Identification of nucleic quasi-primes was performed for kmer length of sixteen bps. This was the shortest kmer length at which we observed DNA quasi-primes. Similarly, for peptide kmers, we performed quasi-prime identification for kmer lengths of six and seven amino acids, since these were the shortest peptide lengths at which we observed quasi-primes.

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