Next Generation Sequencing Library High Impact Factor Journals
Next Generation
sequencing (NGS), hugely equal or profound
sequencing are connected terms that portray a DNA
sequencing innovation which has altered genomic research. Utilizing NGS a whole human
genome can be sequenced inside a solitary day. Interestingly, the past Sanger
sequencing innovation, used to disentangle the human genome, required longer than 10 years to convey the last draft. In spite of the fact that in
genome research NGS has for the most part supplanted customary Sanger sequencing, it has not yet converted into routine clinical practice. The
impact factor of journal gives quantitative appraisal device to reviewing, assessing, arranging and contrasting
journals of comparative kind.
High Impact List of Articles
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