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Next Generation Sequencing Innovations

 The hugely equal sequencing innovation known as cutting edge sequencing (NGS) has reformed the natural sciences. With its ultra-high throughput, adaptability, and speed, NGS empowers analysts to play out a wide assortment of utilizations and study organic frameworks at a level at no other time conceivable.    The present complex genomic research addresses request a profundity of data past the limit of conventional DNA sequencing innovations. Cutting edge sequencing has filled that hole and become a regular examination device to address these inquiries.    Utilizing slim electrophoresis-based Sanger sequencing, the Human Genome Project took more than 10 years and cost almost $3 billion.    Cutting edge sequencing, interestingly, makes huge scope entire genome sequencing (WGS) available and reasonable for the normal scientist. It empowers researchers to examine the whole human genome in a solitary sequencing investigation, or grouping thousands to a huge number of genomes in a single year.    NGS-based RNA-Seq is a ground-breaking technique that empowers scientists to get through the wastefulness and cost of inheritance advances, for example, microarrays. Microarray quality articulation estimation is restricted by clamor at the low end and sign immersion at the top of the line.

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Google Scholar citation report
Citations : 875

BioTechnology: An Indian Journal received 875 citations as per Google Scholar report

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  • China National Knowledge Infrastructure (CNKI)
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  • Cosmos IF
  • Directory of Research Journal Indexing (DRJI)
  • Secret Search Engine Labs
  • Euro Pub
  • ICMJE

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