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Using two different programs we predicted common potential allosteric inhibitor binding sites on both structures.
The automatic assignments of bCSs were done using two different programs, the AutoAssign (Moseley et al. 2001) and the RASPnmr (MacRaild and Norton 2014).
We found evidence of multiple paternity in all 20 broods (Table 2) using two different programs GERUD and COLONY.
Using two different programs to identify transcription factor binding sites in this region of the mouse VEGFA promoter, we were unable to identify any potential ATF6 sites.
The p16 mRNA was predicted to be the target of miR-24 at two sites (CR and 3'UTR) after performing computational analyses using two different programs, Miranda and RNA22.
Assemblies were performed using two different programs: Newbler (version 2.5 beta) and MIRA (version 2).
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A comprehensive bioinformatics analysis using six different programs allowed us to predict putative targets for the two differentially expressed miRNAs identified.
We generated sequence reads from four species and mapped them either to the transcriptome or genome using six different programs: BLAT [12], SSAHA2 [13], Bowtie [14], SeqMap [15], MAQ [16] and CLC NGS Cell [www.clcbio.com].
We called SNPs using three different programs as described below.
Significant evidence of selection was sought using three different programs: PAML, ADAPTSITE and SWAPSC.
Homologous sequences were then aligned using three different programs: MUSCLE v3.7 [ 72], MAFFT v6.712b [ 73], and DIALIGN-TX [ 74].
More suggestions(15)
using two different bits
using two different medications
using two different processes
using two different strategies
using two different lots
using two different routes
using two different products
using two proprietary programs
using two different instruments
using two different methods
using two different procedures
using two different paradigms
using two different weights
using two different possibilities
using two different sources
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