Sentence examples for opportunity to sequence a from inspiring English sources
Azolla will provide a novel opportunity to sequence a plant nuclear genome that has co-evolved for more than 70 million years along with the genomes of its obligate, vertically-inherited symbiotic microbiome.
High-throughput next-generation sequencing (NGS) provides an opportunity to sequence and analyze genomes of multiple species from an environmental sample without cultivation.
However, the advent of Next Generation Sequencing (NGS), by decreasing sequencing costs of a factor 1,000 [ 1], provided the opportunity to sequence the genomes of new organisms (new-models) at different stages of completion.
Single cell experiments provide an unprecedented opportunity to reconstruct a sequence of changes in a biological process from individual "snapshots" of cells.
By providing students with the opportunity to use a sequencer and sequence novel organisms, some of the mystery of sequencing was removed and the students were motivated to explore the complex data.
The availability of large collections of Expressed Sequence Tags (ESTs) for the Solanaceae now provides the opportunity to assess sequence conservation and divergence on a genomic scale.
Having parallelization handled at the algorithm identification level creates an opportunity to revisit sequence analysis for additional fragmentation into map-reduce patterns functions.
When handled properly, the identification of precursors provides an opportunity to interrupt an accident sequence from unfolding; when ignored or missed, precursors may only provide tragic proof after the fact that an accident was preventable.
The maternal mode of inheritance for mtDNA (Giles et al, 1980) and high variability in sequence offers the opportunity to be a more sensitive method (Salk and Horwitz, 2010).
The recent development of faster pulse sequences provides an opportunity to provide a movie of cine images [ 37].
However, EST-SSRs represent a unique opportunity to exploit existing sequence information and by-pass creation and sequencing of SSR-enriched (or random) genomic libraries.
