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To date, a number of genetic maps have been constructed using single dose (SD) markers.
Probe-based dual electrode systems have been constructed using single and dual barrel (theta) borosilicate and quartz pipets as a scaffold.
Genetic linkage maps have been constructed using single dose restriction fragments (SDRFs), SSRs, sequence-tagged sites (STS) markers, expressed sequence tags (EST -derived SSRs, gEST -derivedSSRsmarkers, and diversity array technology (DArT) markers [ 97- 101].
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These plots can be constructed using single or combined measures of diversity.
High-density map of genome-wide graphic genotypes was constructed using single nucleotide polymorphism SNP markers as described previously (Gao et al., 2013).
The performance of AMS 4.0 is compared with the accuracy of previous versions, which were constructed using single machine learning methods (artificial neural networks, support vector machine).
Input output curves (stimulus intensity versus dopamine release) were constructed using single, constant current pulses (0 250 µA, 1 ms duration) delivered between voltammetric scans.
To study segregation distortion in wheat, a high-density consensus map was constructed using single nucleotide polymorphism (SNP) and simple sequence repeat (SSR) markers by merging two genetic maps developed from two recombinant-inbred line (RIL) populations, Ning7840 × Clark and Heyne × Lakin.
More recently, dense linkage maps have been constructed using Simple Sequence Repeat (SSR) [ 12- 16] and Single Nucleotide Polymorphism (SNP) [ 17, 18] markers.
Large single layer sheets of highly ordered array have been constructed using a supporting lipid monolayer.
In the MINIMAX_BSC, items are initially divided into groups and multiple tests need to be constructed using a single item from each group, while minimizing differences among the tests.
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