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Using rationally designed short peptide sequences, we determined that the charge type and identity of amino acids surrounding FG sequences impact the structure and selectivity of FG-based gels.
By comparing the genomic and the cDNA sequences, we determined the organization of the Medaka fas, fadd and casp8 genes.
By comparative analysis of human and rodent Par-4 sequences, we determined the human phosphosite orthologs of rodents S124 and S223.
From the orthologous sequences, we determined the most common set of transcripts of zebra finch which is present in all species or most of the species.
The last exon sequences we determined are available as Additional files 1, 2, 3. PCR was used to amplify rhesus macaque genomic DNA using human primers.
By comparison of the genomic and cDNA sequences, we determined the number of exons and the exon-intron boundaries in these three genes.
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Upon cloning and DNA sequencing, we determined that the 2.1- and 1.6-kb fragments contained ALV-J gp85- and gp37-like sequences.
Both of these differed from the SC5314 sequence we determined by the same two point mutations.
For each sequence we determined the number of repeat-induced gaps at a number of read length benchmarks.
By Sanger sequencing, we determined consensus whole-genome sequences for A/H1N1pdm viruses sampled nationwide in Canada over 33 weeks during the 2009 first and second pandemic waves.
For each flanking sequence, we determined whether it intersects a repetitive element, and the percentage of sequences with an intersection was computed amongst all 40 flanking sequences.
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CEO of Professional Science Editing for Scientists @ prosciediting.com