Sentence examples for sequences are enriched from inspiring English sources

Recent findings indicate that repetitive sequences are enriched in chromosome-associated non-coding RNAs, and repeat-rich RNA shows unusual properties, including localization and stability, with similarities to XIST RNA.

Recent in silico prediction of cis-sequences over-represented in Fe deficiency-induced gene promoters revealed that the IDEF1-, IDEF2-, and OsIRO2-binding sequences are enriched within the 500-bp promoter regions of Fe deficiency-induced genes (Kakei et al. [2013]; Ogo et al. [2014]).

These findings led us to hypothesize that in many cases, Cdk substrates might contain clusters of phosphorylation sites, and therefore that Cdk substrate prediction could be improved not only by optimizing the consensus motif sequence, but also by following consensus site identification with selection of proteins whose sequences are enriched for repeats of that motif.

Second, both proteins display efficient binding to collagens [7], [9] Third, the collagen sequences recognized by LAIR-1 and LAIR-2 (as determined using the collagen tool-kits) overlap to a significant extent and collagen-binding is in both cases more efficient when the sequences are enriched in Glycine-Proline-Hydroxyproline (GPO -triplets [10].

Even though the majority of ESEs have been found in enhancer-dependent introns containing a weak splice site, their discovery in constitutive exons [28] [33], together with the finding that protein-coding sequences are enriched for potential SR binding sites [34] [37], suggests that they could be present in the majority of exons.

The NR patent sequences are enriched with biological annotation and additional data from patent documents.

With each round of Neutral SELEX, sequences became less stable and changed in nucleotide content, but no sequences were enriched.

Among 30 mouse MsrB1 ESTs, Form 1 sequences were prevalent in samples from C57BL/6 mice, whereas Form 2 sequences were enriched in FVB mice.

In this study, functional SH3 sequences were enriched from a SH3 RNN 28 library but not from a SH3 YNN 28 library even after additional 2 rounds of selection.

Consistent with this observation, the TAR-deduced peptide sequences were enriched for GC-rich codons, such as Pro and Arg (Figure S6).

These results suggest that the functional SH3 RNN 28 sequences were enriched earlier than the functional SH3 NNN 28 sequences, and it presumably caused recombination between the formerly enriched sequences in the SH3 RNN 28 library during PCR.