Sentence examples for workflow sequence from inspiring English sources

In the PGM workflow, sequence data were aligned with TMAP [ 26] and variants called using the variant caller v4.0.

TMA workflow (sequence of cores viewed) was also facilitated within Distiller, thereby eliminating the risk of reporting error when performing the digital TMA review.

ProSeq3 supports and facilitates all steps of DNA sequencing workflow from sequence chromatogram editing to DNA polymorphism analysis of multigenic data.

This architecture is substantially different from other information management solutions created for NGS data that are oriented to sequencing facilities, such as the Galaxy LIMS [ 14] which handles requests from users to the service, or the NG6 [ 13] that controls the sequencing workflow at sequencing providers.

Failure to rationalize the non-unique variability within the context of unique stratal geometries is counterproductive, and obscures the simple workflow of sequence stratigraphy.

The AGeS server comes preconfigured with the Jetty Web server [23] and uses Apache Derby [24] as the embedded relational database management system (RDBMS) to provide persistence support for workflow and sequence annotation data.

An overall workflow of sequence analysis performed in this study is encapsulated in Figure  2.

Here we present a high throughput workflow to sequence genomes of large number of yeast strains at a low price.

SIMPLEX [ 60] is an autonomous analysis pipeline for the analysis of NGS exome data, covering the workflow from sequence alignment to SNP/DIP identification and variant annotation.

'SIMPLEX' [ 140] is an autonomous analysis pipeline for the analysis of NGS exome data, covering the workflow from sequence alignment to SNP/INDEL identification and variant annotation.

We apply this workflow to sequence the protein-coding regions of 15 genes in which loss-of-function mutations cause recessive Mendelian disorders often included as part of routine carrier screening, and demonstrate through realistic simulation and comparison with Sanger sequencing data that our approach achieves high accuracies and detects the vast majority of disease-causing mutations.