Sentence examples for assignments putative from inspiring English sources

For definitive assignments, putative identifications should be validated against standards with retention time and MS/MS matching.

Finally, each Fosmid Figure is accompanied by an abbreviated spreadsheet that provides information about the annotated gene sites, including strand assignments, putative start and stop codon sites, and putative gene product identity.

All Illumina assembled unigenes (consensuses and singletons) longer than 200 bp were annotated by the assignments of putative gene descriptions, conserved domains, Gene Ontology terms, and putative metabolic pathways to them based on sequence similarity with previously identified genes annotated with those details.

The taxonomic assignments of putative mRNAs were predicted using the MEGAN software at the family level [56].

We describe here an NMR-based approach for rapidly and reliably testing functional assignments of putative enzymes.

Nevertheless, the genomic synteny of nif genes across nitrogen-fixing species facilitated in silico assignments of putative sequences involved in nitrogen fixation.

These detailed annotations were valuable in the assignments of putative functions (gene names and 'CDS' or protein sequences) to the unigenes.

Sequences were depleted of chimeras and assignments to putative species (>97% similarity) were done with BlastN [ 58] against a manually curated database compiled from NCBI by the Research and Testing Laboratory (Lubbock, TX) [ 38].

Here, we describe the use of nuclear magnetic resonance (NMR -based ligaNMR -basedng as a tooligandtescreeningctionas assignmentoolforutestingenzymes that may be ofunctional reliassignments

Examples of gas chromatography/mass spectrometry (GC/MS) and liquid chromatography/mass spectrometry (LC/MS) data, as well as a list of identified compounds, are provided in the Supporting Information; note that chemical identification assignments are putative with varying degree of certainty.

The nucleotide sequences were examined for sequence variations (in particular deletions and insertions that may disrupt genes and/or lead to frameshifts or premature termination of translation) and incorrect initiation codon assignments with putative ribosomal binding sites also being taken into account.