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We obtained ~500-fold coverage of reads.
Transcript abundance is inferred through normalized fold coverage of reads mapped to the species transcriptome [ 57].
Finally, there is finite coverage of reads for any particular SNP.
This value is then scaled by the fractional coverage of reads for a particular scaffold.
High coverage of reads successfully supported for the following DGE analysis.
Edges are weighted using contig coverage (not coverage of reads used for the assembly, but coverage of seed-reads, which represent more reliable reads).
Firstly, the total coverage of reads from the 5′ to the 3′ end of genes was examined.
RepConsensus is a package independent of RepEnrich that can be used to visualize coverage of reads along a consensus element.
Genome coverage of reads mapping to genes, antisense, and sRNAs were calculated using BEDtools (Quinlan and Hall 2010).
Here, y indicates the coverage of reads that are 100% identical to the reference sequence at the position.
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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