Al Mavahibul Jaliyya Full Pdf 31

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This procedure results in a library that is composed of elongated unnatural strands (i.e., fragments containing unnatural nucleobases) in the selected sequence. The final library is SBS-compatible and ready to be used in Illumina sequencing.

The sequence reads from each channel are extracted and stored in a data processing pipeline. The first step is the removal of the adapters that flank the sequences of the DNA strand. The adapter-cleaned sequences are mapped onto the reference genome (human or bacterial) using the SOAP alignment program [35]. Afterward, the reads are trimmed by the sequence of the molecule and the reads from each channel are merged to obtain the read pairs. The reads that overlap on the same molecule are deemed to be the same clone, and the merged reads are the same as a set of template molecules which, for a known template molecule, is called a gene fragment (gene fragment, hereafter). 827ec27edc