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In our work, bioinorganic assemblies are generated from the cross-linking of Au nanoparticles with either native or mutant phage through electrostatic interaction of the pVIII major capsid proteins (pVIII).
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De novo assemblies were generated from all raw sequence data.
For the E. aphyllum sample White Sea, which was sequenced using both the HiSeq 2000 and MiSeq, independent assemblies were generated from the read sets.
The neutron source driving the sub-critical assembly is generated from the interaction of 100 KW electron beam with a natural uranium target.
An assembly was generated from these reads with Velvet [ 43], using the wMel genome as a reference.
This assembly was generated from 7,615 BAC clones, which were fingerprinted and then arranged into contigs by overlap analysis to generate a physical map.
The 472 Mb sequenced assembly was generated from DH-Pahang, a doubled-haploid genotype, obtained from the Musa acuminata subspecies malaccensis accession 'Pahang' (523Mb 1C estimated size).
A 202-Mb draft genome assembly was generated from P. obducens using Illumina technology and mined to identify 13,483 SSR motifs.
A single representative de novo assembly was generated from a concatenation of the four libraries using the Trinity pipeline (r2014_07 17) [ 5, 6].
A de novo assembly was generated from these sub-reads using the Hierarchical Genome Assembly Process HGAPP) version 1.0 [ 44], with the genome size parameter set to 1.2 Mb.
If S. tropicalis has a large female-specific genomic region on the W chromosome, we expected a higher proportion of the Illumina reads from females to map to the genome assembly because this assembly was generated from a female individual.
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