Your English writing platform
Discover LudwigSuggestions(3)
Exact(7)
Warning: the blog post you are about to read contains some serious, soul-searching reflection.
Only a single normally spliced read contains the G→T mutation.
G C is a graph with a vertex for each SNP and an edge between two SNPs if at least one read contains both SNPs (Fig. 2).
Each MiSeq sequencing read contains a 4-bp multiplexing index, 18-bp PCR primer sequence, 20-bp barcode, 26-bp universal spacer, and 33-bp flanking genomic sequence.
The paired-end reads for each of the 96 samples were pre-processed in order to discard any pair in which at least one read contains one or more ambiguous bases.
Given a target length t, the putative trimming to length l would give a length threshold score: The second factor models 'coverage', and provides a linear score based on retained sequence length: This reflects that, given reasonably high-accuracy bases, a longer read contains more information that is useful for most applications.
Similar(53)
Each sequence read contained data for >855 (5 × 171) nucleotides.
The data were cleaned by removing reads containing adapter, reads containing poly-N, and reads of low quality.
In this step, clean data (clean reads) were obtained by removing reads containing adapter, reads containing ploy-N and low-quality reads from raw data.
The combined collection of Titanium reads contained 1,071,556 reads and 393,338,082 bp with an average read length of 367 bp.
(2) exact barcode matching, two nucleotide mismatch in primer matching, reads containing ambiguous characters were removed.
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