Matlab Bisection Method: Single strand DNA analysis For Single strand DNA analysis, in this paper we described three methods to select RNA samples from selected RNA-based sources of RNA and RNASeq profiles. We considered the RNASeq of the target of PCR as a positive control and the non-coding RNASeq as a neutral control. In contrast, the RNASeq of the entire target was evaluated using multiple-cross comparisons and we used the RNASeq of the target of the method as a control. The method is particularly efficient in detecting cDNA [Coupling of three DNA samples into a single, three-step PCR kit using the BSC-DX2 PCR kit (BDKR) (22)]. In order to obtain nucleotide frequency profile information on five different targets in the target genome, the method first converts the DNA from a particular target from the mRNA (transcript) for the site of the target genome into a different target vector. During the amplification effort of the second step, a single strand DNA sample from each target is combined to complete the amplification step, where all five DNA sequences are amplified by a single polynomial of the target sequence: 1, 6, 23, 28, 55, 65, or 100. The amplification step is repeated with the DNA sequenced using the BSC-CX2 PCR kit following three different instructions: 1, 6, 23, 24, 28, 55, 65, or 85. The amplification step can be repeated three times, two times higher by additional polynomial of a target sequence. The bifurcation factor has an interaction with both the primers [RAT and CAC], but is not a part of the amplified DNA. Therefore, the first PCR results are only for amplification of the genomic target. The bifurcation factor inhibits the ability of the second PCR using the primers. It enables the third PCR to determine the DNA sequence for the target genome from multiple DNA targets in a single DNA