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This version was used to map the sequences around small RNA reads to identify structures consistent with miRNA precursors (according to prediction programmes detailed below).
Eland_extended algorithm was used to map the sequences to human genome (hg18).
To integrate this genetic map with the BAC-based physical map, the sequences of genetic markers were aligned with BES from the physical map using BLAST.
BLAT was used to map the sequences to the reference genome.
Using the genetic map, the sequences were assigned to the north euchromatin, the heterochromatin, or the south euchromatin.
For such a large number of the sequences, BLAST tools are too slow to map the sequences to target genomes.
Similar(49)
We are also developing biophysical models that can map the sequence of a genetic part (e.g., a ribosome binding site) to its function.
Longitudinal investigations using structural magnetic resonance imaging (MRI) provide a framework to map the sequence of neuroanatomical changes at all levels of this model.
The second approach attempts to map the sequence reads to a position within a reference genome.
In this study, we map the sequence reads to pre-miRNAs rather than the mature miRNAs.
Consequently, almost all whole-genome sequencing projects map the sequencing reads onto the human reference genome sequence without performing whole-genome assemblies (Ley et al. 2008).
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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