Sentence examples for identified to reside from inspiring English sources

Of the 153 SSR markers identified to reside closely with these genes, 22 (14%%) exhibited clear polymorphism between the two parents.

Additionally, two novel genes, GRIN2D-1_Ol and GRIN2D-2_Tr, were identified to reside in the medaka Chromosome 11 and fugu scaffold_202, respectively.

One novel GRIN2C_Gg gene was identified to reside in the chicken Chromosome 18. Due to the sequenced gap of this location, however, only 7 exons were obtained using GENSCAN prediction.

The resolution of the system has been measured by distinguishing 1 μm fluorescent beads and was identified to reside on the sub micron range.

The SGCE gene previously reported to be up-regulated in HCC by our group [ 19], was identified to reside within an amplicon at 94,187,248 bp--94,227,832 bp of 7q21.3.

The importance of Wnt signaling in bone diseases has been recognized since the rare human mutations affecting bone negatively (osteoporosis-pseudoglioma syndrome) or positively (high-bone mass phenotype) were all identified to reside in components of the canonical Wnt signaling machinery a decade ago.

Most of the bacterial species identified are known to reside in the vaginal, gastrointestinal or respiratory tract.

Seven (H5, H9, H10, H11, H16, H17, and Hdic) of the 35 resistance genes heretofore identified were reported to reside on the short arm of chromosome 1A and confer resistance against biotype GP [ 3, 7- 11], and four of them (H9, H16, H17, and Hdic) also confer resistance against Hf biotype L, the most virulent and prevalent biotype in the eastern USA [ 1].

Mapping between the sequences identified and predicted miRNA genes was shown in Additional file 5. Thus, six newly identified miRNAs were found to reside between protein-coding genes, eight in the antisense strands of introns and 10 within introns.

The 197 identified proteins predicted not to reside in cytosol are all very low abundance proteins representing less than 5% of the protein copies of the cell even if the most stringent criteria are applied and ribosomal proteins are excluded.

Genetic mapping and exome sequencing identified the potential causative mutation to reside in the CLTCL1 gene encoding CHC22, the second clathrin heavy chain protein.