Sentence examples for grade sequence from inspiring English sources

Proteins were then digested with 1 μg trypsin (Porcine Prep Grade Sequence, Promega - Madison, WI, USA), in 1 mM calcium chloride) at 37°C overnight.

Clinical grade sequence analysis using SNaPshot on DNA extracted from bone marrow and extramedullary plasmacytomas is feasible and leads to the detection of potentially druggable mutations.

Nebula will offer a "1x whole genome sequencing," which provides more data to future researchers than genotyping, but is less detailed than a clinical grade sequencing, which today costs about $1,000 and is used for diagnostics and medical recommendations.

A sharp upper boundary separates it from a massive layer of loamy carbonate sand (0.60 0.35 m b.s)., which is divided into three subunits: (i) a lowermost normally graded sequence with shells and shell fragments (0.60 0.50 m b.s).; (ii) a coarsening-up sequence (0.50 0.43 m b.s).

These assemblies were subjected to near 'comparative-grade' sequence finishing as described in Blakesley et al. [ 26].

Most disappointing was the fact that many troublesome gaps in the Sanger-derived assemblies, which had been extremely problematic (and expensive) to close during human-grade sequence finishing, remained unchanged following the incorporation of Velvet-assembled contigs.

Furthermore, generating the sequence of regions within captured gaps (e.g., during human-grade sequence finishing) is most readily achieved by sequencing the spanning plasmid subclones; in contrast, generating the sequence of regions within uncaptured gaps requires sequencing alternative templates (e.g., PCR products or purified BAC DNA), which is more costly and labor-intensive.

A series of thin normally graded sequences may only be attributed to one single storm event if the graded layers are not separated by mud layers due to the short periods of storm wave pulses (Morton et al., 2007).

Most of the graded sequences start with a sudden increase in Ca, which gradually decreases upwards (Fig. 7).

We measured sequencing error in the newly available low-coverage (∼2×) genome by comparing them with corresponding "comparative-grade" sequences from the ENCODE project [23], [24] (Table 1).

We fully expect that the barrier to the clinical-grade sequencing of germline genomes, preferably from blood-derived DNA, will be substantially lower in 12 months' time, thus allowing a huge increase in such sequencing to occur.