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*Partek percentages are lower as the program was used to define transcripts in very limited regions.
The MUMmer program was used to define conserved genomic regions, inversions, and translocations between the two genomes.
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Subsequently, the Humphrey central 30 2 full-threshold program (C30-2 program) was used to determine the visual field, which was defined as reliable when fixation losses, false-positive errors, and false-negative errors were less than 20%.
The Bayesian algorithm of the program structure was used to define genetic groups within Hawaiian Metrosideros and the closely related taxon M. collina from the Marquesas and Austral Islands.
With masked genome sequences, the BLASTZ alignment program [49] was used to define the map of conserved synteny using the "C = 2 T = 1 H = 2200 Z = 10" option to align each of the genomes to the Pig sequence.
In two studies RTOG-85-31 RTOG-85-31 RTOG-85-31ng was usEPCto define nodal involvement associated with malignancy.
Initially, the program phasing was used to define the marker phases in each family in the pedigree.
The program STRUCTURE was used to define the population structure and identify the ancestral sources of the 10 gene fragments from all the strains.
The program SOCKET [29] was used to define the beginning and end of coiled-coil motif.
A spatial analysis of molecular variance, as implemented in the program SAMOVA 1.0 [ 117], was used to define partitions of sampling sites that are maximally differentiated from each other without any a priori assumption about population structure.
The program BLAST 2 Sequences [ 22] was used to define the conserved regions in each pair of homologenes.
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CEO of Professional Science Editing for Scientists @ prosciediting.com