Sentence examples for duplication call from inspiring English sources

We observed an average of 83 SNPs throughout the duplicated region in these ranges which are all highly supportive of a duplication call.

BAF values in this range make the duplication call very clear for both a HMM algorithm and a graphical review.

To gain further confidence in the duplication calls on 5q35.1, we extracted and viewed BAF and LRR values derived from the Perlegen 600 k data for the CNV region and flanking diploid regions (Figure 2).

To test this, we applied hierarchical clustering to 11 944 high-quality germline deletion and duplication calls (≤1 Mb).

LINE insertions are flanked by 10 20 bp long duplications called target site duplications (TSD).

These findings led to the idea that, after genome duplication, duplicated genes (called ohnologs when originating in a genome duplication) are redundant, so some of their ancestral functions like expression domains, protein functional domains, or protein quantities can reciprocally degenerate.

Among massive duplicated genes of S. cerevisiae (most of which were formed by whole-genome duplication, and called ohnologs-a subset of paralogs), many gene pairs were combined into a network system specially involved in oxygen response.

That art should be an outright duplication (incorrectly called "imitation") of reality is a view that was put forward by the French novelist Émile Zola (1840 1902) in his book Le Roman expérimental (The Experimental Novel) and has been occasionally held (though not practiced) by painters reacting against Romanticism, such as the 19th-century French artist Gustave Courbet.

Two paralogous chromosomes or genes arising from a whole genome duplication are called ohnologous.

Sonnhammer and Koonin developed related terms to describe in-species duplication events (called 'inparalogs') and other types of paralogy [ 31].

The MYD88 L265P mutation in the discovery case with the 3q duplication was called in only one third of the reads (14 of 50) by the WES analysis, so likely the mutation is located on the non-duplicated region of chromosome 3. Somatic mutations identified in the discovery cases are shown in Table  2.