I'm having a hard time to find how to merge my data when I have a single nucleotide variation. How can I tell my Rstudio script to merge my data when I have only a single nucleotide variation (that I consider due to a PCR bias amplification of my library) ? I would like to merge the data to rows that have the highest clonal rate, like this :
0.3520491020252197 TGTGCCAGCAGTTTGAATTTAGCGGACGGTGAAGCTTTCTTT 0.0324321742453190 TGCGCCAGCAGTTTGAATTTAGCGGACGGTGAAGCTTTCTTT
so I have :
cloneFraction nSeqCDR3 0.38448.... TGTGCCAGCAGTTTGAATTTAGCGGACGGTGAAGCTTTCTTT
Thank you for your help, I know how to merge but I'm looking on how to tell the script to merge when only one nucleotide is different.