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From the canine genome database and its bioinformatic analysis, we identified conserved sequences within the vast majority of 61 variable segments and 1 joining segment of the immunoglobulin heavy chain (IgH) gene, and designed optimal primers for polymerase chain reaction (PCR) amplification directed at these conserved sequences to evaluate the monoclonality of IgH in canine B cell lymphoma.
We use four MVD test sequences to evaluate the performance of the proposed view synthesis method.
[106] recommended to use thin-slice (2 mm) proton density coronal oblique sequences to evaluate LCL and popliteus tendon.
Although dark-fluid sequences have lower contrast between cartilage and fluid than bright-fluid sequences [4, 7], there was no significant difference in the performance of both sequences to evaluate cartilage in our study.
Our dataset consist of two datasets from different retinal image modalities such as color fundus images and the corresponding RF, AF images, and FA sequences to evaluate the proposed method.
Catheters (with metallic, MR-safe obturators) were implanted by removing the scanner table from the scanner isocenter, inserting the catheter, advancing the table back to the isocenter, and then re-acquiring FSE sequences to evaluate the catheter positions (on both axial and sagittal planes).
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Synthesized clinical data with whole exome sequencing to evaluate patients with undiagnosed diseases.
Giannopoulou, E. G., Elemento, O. & Ivashkiv, L. B. Use of RNA sequencing to evaluate rheumatic disease patients.
All individual fastq sets were concatenated based on biosample id and results were compared to those reported by the authors who used qPCR and sequencing to evaluate the samples.
Next, we use chromatin immunoprecipitation followed by sequencing to evaluate the chromatin state of cis-regulatory elements (promoters and enhancers) and view how these elements evolve and influence various muscle repair and regeneration transcriptional programs.
We performed sequential genome-wide linkage analysis and whole-exome sequencing to evaluate participants from family DUK6524.
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