Sentence examples for markers were sorted from inspiring English sources

and even the markers were sorted by color.

Specific cell subsets defined by their cell surface markers were sorted by ARIA cell sorter (BD Biosciences).

Pairwise analyses were performed and markers were sorted in linkage groups at a minimum LOD score of 4.0.

The imputation procedure was: (1) for marker matrix M, markers were sorted from lowest to highest percent missing and missing values were imputed using MNI.

As the grandparent genotypes were unknown, pairwise analyses were performed, and markers were sorted into linkage groups at a minimum LOD score of 4.0.

The expression of cancer stem cell markers (CD166, CD44, and EpCAM) was analysed and populations of cells expressing the markers were sorted using a fluorescence-activated cell sorter (FACSAria III, BD Biosciences).

We originally planned to select SNPs with P-values < 0.01 (-log10(P) > 2), and we found that about 500 SNPs met this condition for the 29 traits (the -log10(P) values at the 500th marker were sorted into descending order for the 29 traits and ranged from 2.089 to 2.421).

Specifically, the LFDRs for each marker are sorted in ascending order.

As a third independent marker, we performed a combined analysis of two regions of the mitochondrial genome: since haplowebs are not suited to analyze non-recombining markers, individuals were sorted into four haplogroups according to their mitochondrial sequences.

After filtering low-quality SLAF markers, segregation distortion markers and other markers that were not suitable for map construction, 13,635 polymorphic markers were obtained and were sorted to five segregation types (ef × eg: 962, hk × hk: 1,046, lm × ll: 3,501, nn × np: 8,123 and ab × cd: 3).

To perform smoothing, raw P values for each marker from the mixed model were sorted by chromosome location.