Sentence examples for microsatellites compared to from inspiring English sources

hMLH1 deficiency revealed 11 (5.91×10−4) and 15 (2.18×10−4) times higher mutation rates for the TGFBR2 and ACVR2 microsatellites compared to hMSH6 deficiency, respectively.

ESTs of cucumber were less frequent in microsatellites compared to genomic sequence, with trinucleotides strongly predominating in the formers.

The CDS of loblolly pine is depleted in microsatellites compared to the full genome, but is denser in hexanucleotides and almost equal in trinucleotides.

Further, the relative frequency and distribution of different SSR motifs in coffee genome indicated coffee genome to be relatively poor in microsatellites compared to other plant species.

Coding regions (ESTs) of the cucumber genome had fewer microsatellites compared to its genomic sequence, with trinucleotides predominating in EST sequences.

The high level of variability for microsatellites compared to other genomic regions [ 1- 4] and their abundance in diverse genomes [ 5- 9] have led to their use as markers in many settings, including linkage analysis [ 10- 14], forensic investigations [ 15- 21], human population genetics [ 22- 27], and phylogeny reconstruction [ 28- 30].

Secondly this may be due to the higher power for detecting LD when using markers with many alleles (e.g., microsatellites) as compared to biallelic SNP markers [ 37].

A reduced genetic diversity and increased differentiation at flanking microsatellites when compared to neutral loci is consistent with a selective sweep for resistant alleles at both loci.

The elution profiles for the PCR products from each of the microsatellites were compared to the gel patterns obtained for the same markers using standard denaturing polyacrylamide gel electrophoresis of P-labelled PCR fragments.

There are four potential explanations for the observed departure from the expected pairwise values of FSTnuc: FSTmtDNA :lack of equilibrium, high rate of homoplasy in the microsatellite markers compared to mtDNA (Zink and Barrowclough 2008), large amount of heterozygosity due to highly polymorphic microsatellite markers (Hedrick 1999), and differential dispersal rates of males and females.

However, weaker evidence of native structure was observed using microsatellite data, compared to mtDNA COI analysis.