Sentence examples for mapping samples were from inspiring English sources

The SLAF sequences and the genotype of all mapping samples were given in Additional file 1.

Peptide mapping samples were loaded onto an Agilent SB-C18 2.1 mm × 150 mm column with 100% mobile phase A (0.05% TFA in 98% HPLC H2O/2% acetonitrile) and eluted with a gradient of 0.5%/min with mobile phase B (0.04% TFA in acetonitrile) over 68 min. The flow rate was 0.2 mL/min, and column temperature was set to 50 °C.

The purpose of maximization of J X) is to find the mapping direction, and the final total divergence of mapping sample is the largest.

A change that was present in only one of the mutant plants as compared to a uniform genotype for the rest of the mapped samples was considered to be EMS induced after application of a threshold of GQ ≥ 30.

In order to develop the application rate map, 21 samples were previously taken for analysis of soil fertility.

The elemental analysis and maps of samples were obtained by the energy-dispersive X-ray spectroscope (EDS) system (Thermo Fisher, Noran System 7, United States of America), operated under vacuum.

Effective minority carrier lifetime maps of samples were measured after annealing using the microwave-detected photoconductive decay (μ-PCD) WT-20000, Semilab).

As for proteome map construction, samples were taken during the late fed-batch production phase (around 160 h) for each sample.

Genes with an average of at least one uniquely mapped read across samples were tested for differential expression using QuasiSeq (http://cran.r-project.org/web/packages/QuasiSeq).org/web/packages/QuasiSeq

L* values of coated + MAP and control samples were 68.8 and 48.9 after 8 days storage, respectively.

Those transcripts with no reads mapped in all samples were considered errors and removed.