The phrase "assembly nucleotide" is correct and usable in written English.
It can be used in contexts related to molecular biology or genetics, particularly when discussing the components involved in the assembly of nucleotides in DNA or RNA synthesis.
Example: "The process of DNA replication requires the assembly nucleotide to form the new strands."
Alternatives: "nucleotide assembly" or "nucleotide construction".
ORFs 25, 19, 27, and 38 forming a fully connected cluster in VZV code for proteins involved in virion assembly, nucleotide repair, metabolism, and host-virus interaction.
These clusters contain proteins in different functional classes; one cluster in VZV contains proteins involved in virion assembly, nucleotide repair, metabolism, and host-virus interaction.
This view predicts a semiordered assembly: nucleotide-facilitated formation of G heterodimers (Cdc3– Cdc11/ Cdc11/ Shs1– Cdc12) and nucleotide-independent Cdc3– Cdc12 NC heterodimerization occur simultaneously, followed by NC-homodimer-mediated joining of the resulting Cdc12– Cdc11– Cdc3– Cdc10 heterotetramers into heterooctamers and ultimately into filaments.
Reads were aligned to the reference D. melanogaster genomic assembly, single nucleotide polymorphisms were identified, and nucleotide variation was quantified genome wide.
Eleven genes present in a single copy within Sorghum were matched to the Miscanthus transcriptome assemblies using nucleotide-nucleotide BLAST (blastn).
515 of 168,849 (0.31%) of these nucleotides showed sequence changes, providing an estimate of the assembly's nucleotide substitution errors.
During de novo assembly, two nucleotide mismatches (M = 2) were allowed among reads to form a putative RAD-locus.
At the end of the assembly single nucleotide variations were reintroduced (by mapping back reads) and a mix of both haplotypes was obtained.
Large collections of ESTs enable the assembly of nucleotide sequence contigs and, if the genomic sequence is available, a means of mapping the species genome and ultimately assist in gene and pathway discovery.
For MOR family assignments, we performed a blastn search of each mouse OR we found in the most recent mouse genome assembly against nucleotide sequences of a set of mouse ORs named according to a different classification system [ 73].
ParM, which is the very well characterized actin homolog that is used to segregate plasmids in bacteria [ 31], even shows dynamic instability [ 54], which is one of the classic outcomes of the coupling of assembly to nucleotide hydrolysis for eukaryotic cytoskeletal filaments [ 65, 68- 70].
