Exome sequencing analyzes the protein-coding region of the genome, as a cost-effective alternative to whole-genome sequencing. The HiSeq 4000 System can sequence up to 96 exomes* per run.
Whole-genome sequencing (WGS) analysis of large complex genomes (human, plant, or animal) provides a base-by-base view of genomic alterations to inform studies of disease or population genomics. The HiSeq 4000 System can sequence up to 12 human genomes* per run.
Analyze both coding RNA and multiple forms of noncoding RNA with total RNA sequencing (RNA-Seq) for a comprehensive view of the transcriptome. The HiSeq 4000 System can sequence up to 100 transcriptomes* per run.
Performs read mapping, FPKM estimation of reference genes and transcripts, novel transcripts assembly, variant calling, and optional fusion calling.
Quickly assess novel transcript isoforms and gene expression levels from RNA-Seq Alignment results.
Access the information you need—from BeadChips to library preparation for genome, transcriptome, or epigenome studies to sequencer selection, analysis, and support—all in one place. Select the best tools for your lab with our comprehensive guide designed specifically for research applications.Access Guide