De Novo Assembly and Genomic Structural Variation Analysis with Genome Sequencer FIX 3K Long-Tag Paired End Reads

摘要

The Genome Sequencer FIX System from Roche and 454 Life Sciences is a versatile sequencing platform suitable for a wide range of applications, including de novo sequencing and assembly of genomic DNA, transcriptome sequencing, metagenomics analysis, and amplicon sequencing. The Genome Sequencer FLX enables long sequence reads separated by kilobase distances of genomic DNA. These Long-Tag Paired End reads enable improved de novo assemblies and genomic structural variation studies.