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The same four biological replicates were sequenced for small subunit (SSU) rRNA genes using high-throughput amplicon pyrosequencing.
Two biological replicates were sequenced for each inoculation and timepoint.
Two independent biological replicates were sequenced in parallel.
Two biological replicates were sequenced for each experiment.
Three biological replicates were sequenced for the TRAP-IP and total RNA samples.
Three biological replicates were sequenced for each treatment and at least three plants were pooled for each biological replicate.
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The cDNA library (two independent biological replicates) was sequenced on the Illumina sequencing platform (HiSeqTM 2000).
Three lanes of HiSeq were used and each biological replicates was sequenced in different lanes according to proper blocking and randomization procedures [ 34].
Although each sample (composed of 6 pooled biological replicates) was sequenced once, DESeq was able to estimate gene expression dispersion by assuming that most genes have similar expression across treatments.
Each biological replicate was sequenced twice on separate lanes on an Illumina Genome Analyzer I, producing a total of six replicates per genotype.
Each sample (i.e., biological replicate) was sequenced on a respective Illumina lane with an average of 31 million reads per sample (1 × 54 nucleotides).
More suggestions(18)
biological replicates were collected
biological replicates were analysed
biological outcomes were sequenced
biological replicates was sequenced
biological replicates were grown
biological replicates were performed
biological species were sequenced
biological replicates were conducted
biological triplicates were sequenced
biological replicates were generated
biological samples were sequenced
biological replicates were normalized
biological replicates were done
biological replicates were set
biological replicates were analyzed
biological replicates were measured
biological replications were sequenced
biological replicates were used
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