Sentence examples for multiple chromosomal locations from inspiring English sources

Exact(15)

The lipid methylene signal (1.22 ppm) showed correlations with polymorphic sites at multiple chromosomal locations, with the highest located around the C43 RFLP marker at 92.8 cM on Chr. 5 (rs = 0.66, P < 0.01), and the second highest around R1943 at 123.7 cM on Chr. 8 (rs = 0.58, P < 0.01).

However, our BAC mapping data rule out the hypothesis that CPI-14 is homologous to any of these reptilian sex chromosomes, and instead suggest that the NOR has undergone translocations to multiple chromosomal locations independently in various reptilian lineages.

Many of the BAC clones that hybridized to multiple chromosomal locations localized near the centromeres, providing further evidence for the lack of chromosome-specific repetitive DNA sequences near these regions.

This method uses genetic variations at multiple chromosomal locations and allows generation of sequence data, which are deposited in internet databases for comparison with DNA sequences of other isolates.

Thirty-one BAC clones localized to multiple chromosomal locations in several different hybridization patterns.

3 Multiple chromosomal locations, genes, and genetic polymorphisms have been implicated.

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Similar(45)

(p. 399) Regardless of whether the regulatory elements arise 'de novo' by a few mutations or are pre-existing within TE sequences, the dispersal of expanding TE families throughout genomes potentially allows the same regulatory motif(s) to be recruited at many chromosomal locations, drawing multiple genes into the same regulatory network.

Feschotte (2008) observes … Regardless of whether the regulatory elements arise 'de novo' by a few mutations or are pre-existing within TE sequences, the dispersal of expanding TE families throughout genomes potentially allows the same regulatory motif(s) to be recruited at many chromosomal locations, drawing multiple genes into the same regulatory network.

Complicating factors included fractionation of QTL, pleiotropy or tight linkage of QTL for multiple traits, pericentromeric chromosomal location(s), and/or QTL × E. High-resolution mapping of QTL in this region would be needed to determine which specific target QTL could be useful in breeding cultivated tomato.

The technique leaves no other DNA in the genome, such as marker genes, and can be used serially to effect multiple complex changes in any desired chromosomal locations.

Mtvs are present in the germline of most of the inbred mice and there are multiple proviral sequences found at different chromosomal locations in different mouse strains.

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