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Each of these reads was classified as known miRNA, piRNA, tRNA, rRNA, snRNA, snoRNA, mRNA, genomic sequence or unknown sequences.
Each of these reads represents a uniquely crosslinked RNA molecule.
In each of these reads, there are two continuous strings connected by '−', which indicates missing information.
We determined the allele for each of these reads based on the observed nucleotide at the SNP position.
Each of these reads may represent a section of a genome, and in some cases several reads may represent the same section.
We used these reads as queries for BLAST searches of the human genome and found no sites other than this insertion boundary in the human genome with significant similarity to the full lengths of each of these reads.
Similar(52)
Consensus genome sequences (8176 nucleotides in length) were created from alignments of these reads at each dilution.
A consensus is generated for all the reads in each cluster based on the alignments of these reads to the reference genome.
85.4% of these reads aligned.
A subset of these reads.
Each of these discordant reads potentially predicts an insertion within an interval (the size of the expected fragment length) downstream of the anchor read (relative to its strand).
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com