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Similar EST collections were generated from other Puccinia species [ 15- 21].
aVdLs.17 expressed sequence tag (EST) collections were generated from cultures grown in CM (complete medium), CM + RE (CM amended with root extract), or CM-N (CM lacking nitrogen source).
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The collection was generated from a single starting material, 4,7-dichloropyrido[3,2-d]pyrimidine, which afforded the final compounds after two steps: a sequential or one-pot sequence including selective cross coupling reactions in C-4, followed by the second cross-coupling in C-7.
The FHCRC EST collection was generated from DT40 cells (a transformed bursal cell line) [ 1, 2], along with clones from the bursal EST project [ 7, 8] and the UD activated T cell library [ 9].
A collection of pathways were generated from the second simulation.
Models were generated from the collection of cumulative data.
Besides the isolates, partial ITS sequence data were generated from two fruitbody collections of putative A. sp. nov., one dried (NZFRI-M 5714) and one fresh (NZFRI-M 5810), in order to confirm their identity.
Draft genome sequences were generated from several BGstrains in our collection.
These sequences were generated from the isolates of same location and collection year (Chidambaram/M 3 8)/India/2009, Kadalur-NM(1 4)/India/2009) as presented in Additional file 1: Table S2.
A total of 16 ITS sequences were generated from 11 species of Geoglossum, Trichoglossum, and Thuemenidium, and one ITS sequence (PDD70355) generated from a New Zealand collection was subsequently identified as a species of Microglossum.
Embryos were generated from natural crosses.
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