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Calculate a genome resequencing assembly

This video shows how to calculate a genome resequencing assembly in BioNumerics Seven using a trimmed Illumnina paired-end dataset. The same workflow is applicable to other Next-Gen data read sets.

Sequence read sets

A sequence read set is designed to hold large sets of short reads generated by next generation sequencing (NGS). Base sequences and their associated quality scores are stored for single-end and paired-end reads, originating from various high-throughput sequencing platforms such as Illumina, Ion Torrent, PacBio, Oxford Nanopore, etc.

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Software major version: 
7.x
See tutorials:
Performing a resequencing assembly