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Thus, in many cases, sequences between RNA genes may characterize a species uniquely.
In many cases, sequences were very short therefore matches were also searched in International Wheat Genome Survey Sequence (IWGSS) database.
In many cases, sequences with signal peptides predicted in one strain lack signal peptides in the corresponding proteins in other strains (denoted by †).
In many cases, sequences from multiple individuals of the same species were combined, to allow us to combine data from different genes for the same species.
Additional file 3: Figure S2B shows the gene profile of all targets included in the microarray, which represents in many cases sequences of several transposases of the same IS family.
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In many cases, sequencing gaps prevented any meaningful improvement.
In many cases, sequencing of chromosome ends revealed a mosaic of specific interchromosomal segmental duplications as observed in E. cuniculi.
In many cases, sequence comparison yields multiple hits for one query protein and these hits may have different functions.
In many cases, sequencing of chromosome ends is performed independently using a combination of molecular and bioinformatics methods [ 17– 22].
In many cases, sequence data available prior to the submission of the Anamika et al paper supplies alternate, more conservative interpretations of chimp gene structure.
In many cases sequence identity of ≥ 98%, based on comparison of full-length sequence as described in Table 3, was sufficient to classify cDNA sequences: CH501 as WC1-1, CH496 as WC1-4, CH505 as WC1-9 and CH486 as WC1-11.
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