2. ResultsThe primary analysis of the reads through base calling directly on theMiSeq sequencing reporter (MSR), revealed raw reads statistics and sequence quality assessment as in Table 1. The fastq reads obtained per sam-ple were in paired-end reads labelled as (L001_R1_001.fastq andL001_R2_001.fastq). The project (PRJNA288893) was registered with theGenBank, with BioSample accession numbers SAMN03839381 (root),SAMN03975610 (stem), and SAMN03975611 (leaf). The highest readswere obtained from the root tissues (2,528,030 reads) followed by theleaf (1,372,180 reads) and stem tissues (1,298,892 reads). The GC contentfollowed the same order (52.01, 50.86 and 50.01), respectively. This trendmay not be unusual since the root is closer to the soil microbial communi-ties than other tissues. The higher reads in leaf tissues compared to thestem, may probably be the result of the relatively larger size of leaf tissuesthan the stem tissues, which might harbour more microbial communities.
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