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Protein spots were excised manually and analyzed by LC/MS/MS at the Southern Alberta Mass Spectrometry (SAMS) Centre for Proteomics at the University of Calgary.
The resulting sequences were processed manually and analyzed twice: first by FASTX against a non-redundant protein sequence database provided by the DNA Databank of Japan (version 3.2t09) without an e-value cutoff, then by blast against a merged DNA database provided by the DNA databank of Japan (release 71.0).
The eluent was monitored by a PDA and peaks were collected manually and analyzed by ESI-MS.
At least two annotated genes at each side of R.PabI were obtained manually, and analyzed for methyltransferases.
The recordings were completed by entering the diary information manually and analyzed based on the manufacture's software (POLYGRAM NET™ Version 14.1.1322.287).
HPLC fractions identified as MC were collected manually and analyzed by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), (PerSeptive BioSystems, Framingham MS, USA) as described by Erhard et al. (1997).
Similar(54)
Three fields per sample were manually selected and analyzed using the Hamilton Thorne IVOS computerized semen analyzer (Beverly, MA), with the calibration parameters defined in Table S3.
Sequences were manually edited and analyzed using Sequencher 4.2 software.
The two sequences were manually aligned and analyzed using Bayesian methods.
Data were manually entered and analyzed using the IBM SPSS Statistics Version 20.0 (SPSS, Chicago, IL, USA).
The reconstructed 3D images were then manually segmented and analyzed in their 3D reconstructed orientation.
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