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A semiautomated analysis pipeline was used to identify sequence variants [14].
Gene scanning software was used to identify sequence variation by melt profiling.
All aligned nucleotide sites, including the insertions/deletions, were used to identify sequence polymorphisms at each of the four loci.
A preliminary alignment of the proteins was used to identify sequence gaps that were removed prior to the determination of sequence divergence.
The best aligning outputs were used to identify sequence direction of the unigenes.
The best alignments were used to identify sequence direction and to predict the coding regions of the assembled unigenes.
Similar(46)
99% similarity clusters were used to identify sequences affiliated with a specific organism to eliminate bias induced by Taq polymerase error [44].
In the first approach, the sequence alignment algorithm Mummer [24] was used to identify sequences unique to each NE strain by aligning the draft genomes of CP4 and JGS4143 with the nine reference genomes.
When the human genome became available, identification of all its functional genomic elements still remained difficult, and genomic comparisons have frequently been used to identify sequences with functional potential.
Two analytical approaches can be used to identify sequences genes whose evolution has been driven by environment-specific selection.
The recently assembled Hessian fly genome (www.agripestbase.org/hessianfly) was used to identify sequences of target genes using the tblastn program.
More suggestions(15)
used to determine sequence
used to identify nucleotide
used to ligate sequence
used to assemble sequence
used to search sequence
used to evaluate sequence
used to end sequence
used to identify vehicle
used to perform sequence
used to identify someone
used to study sequence
used to reduce sequence
used to quantify sequence
used to identify god
used to calculate sequence
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