Sentence examples for shared interval from inspiring English sources

Mutation detection by direct DNA sequencing was initiated in the small potentially shared interval between these two families.

These markers defined a potentially shared interval of 361 Kbp containing three genes (3' end of PEX14, CASZ1, SRG [not currently annotated by RefSeq]).

While careful examination of known genes will not be as complicated in small gene poor areas (chr.4p), this process will be more difficult in large gene rich regions, such as the shared interval on chromosome 6p.

For 1368-1 and 333-1, the inferred haplotype producing the largest shared interval was chosen for further analysis.

Only SNPs called in at least two samples were used for imputation, and only called SNPs were used for determination of the shared interval.

The number of shared intervals varied between HGs and the accuracy of the difference ratio is probably higher in HG1-4 due to the larger numbers of shared intervals (Table  5).

The ∑ | LGmax-LGjk| is the absolute value of the length difference of each shared marker interval within a HG between LGs LGmax and LGi and LG max  + Lg i is an additive value of all shared intervals for the ith LG within HG which is used to normalise the difference value ∑ | LGmax-LGjk| [ 33].

To test for a genome-wide difference in sex-averaged recombination rate between population/species, we used two-tailed sign tests contrasting the number of shared intervals greater in length in one map than in the other.

> -wrap-foot> To further analyze this phenomenon, we examine the difference of the lengths of IBD sharing intervals between those inferred as actual IBD and those inferred as background sharing.

For this, the following heuristic is used: 1. Add all maximal cliques to a list L. 2. For all cliques C in L compute the shared overlap interval I C, i.e., the maximal interval that is overlapped by all of the intervals in the clique.

Such a shared chromosomal interval or haplotype, surrounding the actual pathogenic mutation, is typically detected and defined by multipoint linkage and phased haplotype analysis using microsatellite or SNP genotype data.