Sentence examples for genomic data such from inspiring English sources

These genome visualization tools need three types of information: (1) general genomic data such as the genome sequence and gene annotation.

We characterized 50% of cases with specific genomic signatures using an outlier-based approach, which will be strengthened by the integration of different modalities of genomic data such as whole-genome and whole-exome sequences.

Other interesting features can be implemented in sequence trimming procedures where more sophisticated strategies, such as the one implemented to populate the database Selectome [ 73], could be used to improve the reliability of analysis of more complex genomic data, such as from eukaryotic genomes.

From their inception, high-dimensional genomic data, such as obtained through genome-wide expression microarrays, have been used to identify genes that affects survival or tumour reoccurrence time spans among cancer patients (Bøvelstad et al., 2007; Van De Vijver et al., 2002).

We hence developed a purpose-built approach in SPARK to perform machine learning tasks on genomic data, such as clustering of individual genomes.

But he worries that the issue will arise again for other genomic data, such as complementary DNA sequences, where there are as yet no explicit international agreements.

One of the questions that arises when comparing metabolic pathways is whether it is possible to reconstruct robust phylogenetic trees from non-genomic data such as metabolic pathways.

Thus, the operator can create data types relative to clinical events, such as a tumour onset and relapse, alongside genomic data types, such as MAGE standard format [ 43].

All genomic sequence data, such as CpG islands, were downloaded from the UCSC genome browser.

A prerequisite for a performance comparison of genomic microarrays is the availability of a comprehensive method that accounts for specific requirements associated with genomic microarray data such as adjacency of probes and asymmetric y-axis measurements associated with deletions and/or duplications.

The implied 60% genomic coverage is typical in our experience with single-cell genomic data at such depths of sequencing.