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Exact(5)

While for this study we chose IGF2R and BRAF as representative genes with moderately high GC-rich content, there may be sequences of interest that contain more consecutive guanines per stretch (>90% GC).

This reduction occurs in accordance with the ribosome scanning model [ 5] which does not evaluate the ATGs in the downstream region of the TIS where there may be sequences of ATG with the appropriate context to be the TIS.

Alternatively, these may be sequences that are present in only one of the Brassica genomes, or their genome-specific expression may be tissue-dependent (we have analysed only leaf tissue).

This is due to the reduction in the number of samples classified as false positive in accordance with the ribosome scanning model [ 5] which does not evaluate the ATGs in the downstream region of the TIS where there may be sequences of ATG with the appropriate context to be the TIS.

The remaining alignments with P. trichocarpa were of reasonable length (109-438 bands) and identity 84-944%), suggesting there may be sequences from a plant species related to P. trichocarpa in the great tit assembly (oak, beech and hazel are more closely related to P. trichocarpa than ash or sycamore).

Similar(55)

In vitro data suggest that the combined cytotoxicity may be sequence dependent.

To eliminate this problem, several lines may be sequenced to reveal possible identical SNPs or indels that preexist before transformation.

Probable results, which may be sequenced from specific initiating events, are analyzed, and adequate general countermeasures (safety functions) are selected to ensure safety against risks.

This region of β-tubulin may determine the conformation necessary for correct attachment of ODAs, or there may be sequence-specific interaction between β-tubulin and a protein involved in ODA attachment or stabilization.

A set of PCR primers was designed using conserved regions of the PB1 gene to produce amplicons that may be sequenced for identification of similar fish orthomyxoviruses in the future.

These stop codons may be sequencing errors, null alleles or errors in the alignment.

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