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Herein, aptamer and complementary DNA (cDNA) sequences are designed with four thymine bases on 3′ ends.
The active sequences are designed to be complementary to intronic sequences of the primary transcript of the target genes.
The sequences are designed to retain the intrinsic error correction of the standard Carr Purcell Meiboom Gill (CPMG) sequence.
Course sequences are designed to enable students to achieve advanced competence in all skill areas by the end of the third year, and students are encouraged to spend a summer or term in Africa during their language study.
To minimize the channel estimation error, optimal training sequences are designed to exploit full information of the spatial correlation under the criterion of minimum mean square error (MMSE).
In this fascinating hairpin assembly amplification strategy, mismatched base sequences are designed in hairpin H2 to decrease nonspecific CHA products, which reduce the background signal significantly.
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Probes sequences were designed using Beacon Designer (Premier Biosoft, Palo Alto, CA, USA).
Synthetic DNA, with various sequences, were designed and sequenced in the Pyrome sequencer.
shRNA target sequences were designed by Dharmacon and listed below.
Guide RNA (gRNA) sequences were designed using the Deskgen design platform (https://www.deskgen.com/guidebook/advanced.html).html
The visual definitional sequences were designed to provide this foundation of understanding.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com