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The new data was assembled by the United Nations Office for Drug Control and Crime Prevention in Vienna.
A dataset of control animal microarray expression data was assembled by a working group of the Health and Environmental Sciences Institute's Technical Committee on the Application of Genomics in Mechanism Based Risk Assessment in order to provide a public resource for assessments of variability in baseline gene expression.
The sequencing data was assembled by SeqMan Pro (version 7.1, DNAstar Lasergene), and the mutations that were uncovered were identified by comparison with the H37Rv sequences (NC_000962.3) of embB, embA, embC, embR, and ubiA from the GenBank database (http://www.ncbi.nlm.nih.gov/nuccore/NC_000962.3) using the MegAlign (version 7.1, DNAstar Lasergene).
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The optical mapping data were assembled by MapSolver (v0.5).
High-quality data were assembled by Newbler2.6 and the gaps were then complemented by PCR amplification.
The obtained EST data were assembled by the CAP3 program to obtain non-redundant sequences.
Data were assembled by using GenomeStudio Methylation software from Illumina Sann Diego, CA, USA).
Sequence data were assembled by using Sequencher software (Gene Codes Corp., Ann Arbor, MI, USA).
These data were assembled by the National Center for Health Statistics (NCHS) of the Centers for Disease Control and Prevention, with cooperation from the individual states and the District of Columbia.
Final project datasets of combined web, paper and biomechanical data are assembled by transferring data from Microsoft SQL Server to SAS System for Windows (Release 9.3, SAS Institute Inc., Cary, NC, USA).
Raw sequence data were assembled by using Contig Express (Vector NTI suite 9.1; Invitrogen, Carlsbad, CA, USA), and a 351-nt fragment of the nucleoprotein coding sequence was obtained after deletion of primer sequences.
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