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In brief, we first inferred the sex of the sequenced bird samples by comparing the sequencing read depth level between Z chromosome vs. autosomes.
Whole genome shotgun sequencing can be used for reliable variant discovery in a single sequenced individual by comparing the sequencing reads to the final consensus assembly as done with platypus [ 7].
We estimated the accuracy of transcriptional orientation by comparing the sequencing reads with the annotated gene datasets [ 42].
Differentially expressed miRNAs were identified by comparing the sequencing reads with significant correlations (P <0.05 and P <0.01) between the six libraries.
By comparing the sequencing datasets from three tissues, genes which were differentially expressed in the different organs suggest a potentially tissue-specific function.
By comparing the sequencing depth of TE sequences to sequencing depth of unique genomic sequences, we calculate a metric enabling us to estimate the entire TE content of a library, both ancient TEs and relatively more recent, undiverged TEs.
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The specific sequences were subsequently identified by comparing the sequences with the original library sequences using the BLAT algorithm, and the relative distribution was calculated.
By comparing the sequence of DNA letters in each part of the genome with a library of these fragments, annotators can pick out many of the exons.
By comparing the sequence of parents and offspring, researchers could calculate the rate of spontaneous mutations arising in the human genome from one generation to the next.
We can reconstruct the evolutionary past by comparing the sequences of this passed-down DNA because, occasionally, copying errors — mutations — occur between generations, so that within any lineage the DNA sequences change slowly over time.
By comparing the sequences of these DNA ends against a healthy reference genome as well as between the patients' normal and tumor genomes, the researchers could spot rearrangements between chunks of DNA.
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by comparing the ranking
by considering the sequencing
by comparing the sequences
by aligning the sequencing
by dividing the sequencing
by using the sequencing
by comparing the content
by comparing the test
by comparing the spending
by comparing the position
by comparing the radiocarbon
by comparing the judgment
by comparing the maximum
by comparing the similarity
by comparing the coefficient
by comparing the detail
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