In contrast, all 51I 59R 108N triple mutants were associated with a single microsatellite allele at each locus [He = 0.00, 0.00 and 0.00, N = 16, 15 and 26 for the −0.1, +0.5 and −4.4 kb, respectively, heterozygosity across the three loci: (mean±SD) = 0.00±0.00].
We identified the sequences corresponding to 11 polymorphic microsatellite loci used previously to analyze the D. immitis population structure in North America (36) and genotyped our two isolates in silico by counting the predicted numbers of microsatellite repeats at each locus.
Slettan, A., Olsaker, I. & Lie, Ø. Polymorphic Atlantic salmon, Salmo salar L., microsatellites at the SsOSL438, SsOSL439 and SsOSL444 loci.
Slettan, A., Olsaker, I. & Lie, Ø. Atlantic salmon, Salmo salar, microsatellites at the SsOSL25, SsOSL85, SsOSL311, SsOSL417 loci.
Normal microdissected tissue samples for each case were evaluated for informative status with respect to individual alleles for 18 microsatellites at 10 genomic loci 1p, 3p, 5q, 7q, 8q, 9p, 10q, 17p, 17q, 18q.
The Constellation Observing System for Meteorology, Ionosphere, and Climate mission (COSMIC) is formed by six microsatellites at 800 km low Earth orbit (LEO) and a 72° orbital inclination angle.
The F3/C configuration consists of six microsatellites at about 800-km altitude which are placed in 72° inclination circular orbits with a separation angle between neighboring orbital planes of 30° longitude.
In some cases, the expansion of triplet microsatellites at fragile sites caused human mental retardation (8).
We modeled microsatellite evolution as a birth death process on this fixed phylogeny, where birth death indicates the gain loss of microsatellites at a given locus.
In this study, the segmental duplications represent only a proportion of duplications where we find microsatellites at the sequence ends of the duplications.
