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To generate the reverse complement chromatogram, inference was done by: t r a c e b ¯ [ i ] = t r a c e b ¯ [ L − i − 1 ], in which b = { A, G, T, C }, where b ¯ is the complement base of b, L is the sequence length, 0 ≤ i ≤ L-1.
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Classification of chromosome complement based on centromere position at mitotic metaphase followed Levan et al. (1964).
We describe the design and synthesis of a new Tc-99m labeled bioconjugate for imaging activated complement, based on Short Consensus Repeats 1 and 2 of Complement Receptor 2 (CR2), the binding domain for C3d.
In conclusion, we have developed and characterized a new and versatile radiopharmaceutical for the potential of imaging activated complement, based on rCR2, which contains the C3d binding domain of complement receptor 2. It site-specifically incorporates [99mTc(CO)3]+ with excellent efficiency and is stable in serum.
This feature assesses the confidence of reverse complement bases.
This represents 3.7% of the monoploid complement, based on the estimate of a 10 Gb genome size for the decaploid hybrid cultivar R570 [ 6].
DΔ4/pΔ4 splicing exons only conserved positions P5 and P6, whereas dΔ4/PΔ4 showed two recognizable overlapping 5'ss (positions P-4-P-2 and P1-P6) and U1 snRNA sequence-complement base pairing with extension nucleotides [ 42].
Classification of the chromosome complements based on centromere position at mitotic metaphase follows Levan et al. (1964).
This list was analyzed and complemented based on practical experience and based on information on Web application attack methods available in the literature (e.g., [38 40]).
The classification of the chromosome complements based on the centromere position at mitotic metaphase described in Levan et al. ([1964]) was adopted.
For the most ill-conditioned systems, that correspond to the lowest Fourier frequencies, the PCG is replaced by a direct Schur-complement based solver.
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