Your English writing platform
Discover LudwigExact(60)
Previous studies have used the number of sequence reads of a particular miRNA from deep-sequencing as an indication of molecular abundance [ 42].
However, this limitation is compensated for by the much larger number of sequence reads.
Next, we evaluated how the true positive and false positive/negative rates depend on the number of sequence reads.
Re-sampling and adjustment of the total number of sequence reads to identical sequencing depth was done before analysis [47].
SNP discovery in a mapping cross requires a high number of sequence reads per marker for each parent.
A low number of sequence reads may be insufficient to represent the expression pattern of a single sequence.
In such cases, the number of sequence reads required to ensure a 99.9% probability of detection doubles.
A variable number of sequence reads were obtained from each individual due to varying DNA concentration in the initial samples (Fig. 2D).
Every base of the genome was assigned the total number of sequence reads overlapping it, separately for the input and genomic sequence reads.
With the number of sequence reads being proportional to the transcript abundance, it is possible to make reliable absolute quantification of transcripts.
Despite experimental procedures that we establish to enrich for RNA viruses, a significant number of sequence reads mapped to DNA viruses both ssDNA and dsDNA.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com