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All sequence reads that passed this filtering process were then mapped to the human genome.
All sequence reads that passed this filtering process were then mapped to the human genome with 895 9800 reads, per library with features of predicted novel miRNAs.
Only 1 SNP (less than 1.5% of the variants detected in each individual, and around 6% of the variants shared by the same family) per family on average passed this filtering process, showing that, even after using restrictive thresholds, additional information has to be used to select the most probable variants (Table 5).
Genes that passed this filtering were analyzed further.
Five thousand six hundred and thirteen molecules passed this filtering process.
However, as further analysis revealed the sequences that passed this filtering still contained some mitochondrial contamination.
Similar(50)
A total of 7463 indels and 188,078 SNVs passed this filter.
Phosphorylated peptides which passed this filter were examined manually and accepted only, when b- or y- ions confirmed the phosphorylation site.
10,980 promoter passed this filter.
177 genes passed this filter.
Only 115 CGC genes passed this filter.
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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