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Performance data of these technologies are based on an extensive review.
These technologies are based on hollow cathode discharge (HCD) plasma process rather than the conventionally used glow discharge process.
Because these technologies are based on the expression of fusion proteins, their application can be extended to other biologicals and can be delivered by gene therapy.
Some of these technologies are based on the so-called nanopores (Table 2).
These technologies are based on engineered nucleases that cleave DNA in a sequence-specific manner, thus enabling targeted genome-editing.
These technologies are based on the use of proton emission during polymerization of DNA in order to detect nucleotide incorporation.
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The development of these technologies is based on some biological facts.
The identification of variants with these technologies is based on comparing the reads produced by HTS platforms with the haploid sequence of the human reference genome and finding the bases that differ from the reference genome sequence.
These new technologies are based on different principles than the classical Sanger-based method [ 5], and they are collectively referred to as either 'next-generation' sequencing, 'high-throughput' (or even 'ultrahigh-throughput') sequencing, 'ultra-deep' sequencing or 'massively parallel' sequencing.
These new technologies are based on sequencing-by-hybridization [ 3], sequencing-by-ligation [ 4] or sequencing-by-synthesis [ 5, 6].
These second-generation technologies are based on marrow-derived MSC, and use modern tissue engineering technologies, such as growth factors and scaffolds, to augment and facilitate chondrogenic differentiation for both qualitative and quantitative improvement of repair cartilage tissue.
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CEO of Professional Science Editing for Scientists @ prosciediting.com