Preview of the new BD Genomes website. Yellow boxes are details still to be confirmed.

Sequencing services

Six service areas covering a single gene to a whole genome. Not sure which one you need? Message us — we will help you choose.

Sequencing platforms

Short reads, long reads and capillary sequencing, chosen to fit your project and budget. Client: confirm which platforms are run in-house and which through partner facilities

Capillary

Sanger

For single genes, confirming NGS variants, detecting minor alleles down to about 5%, and reads up to 1,000 bases. Also fragment analysis (genotyping, STRs).

Short read

Illumina NovaSeq 6000

80 Gb–6 Tb output, 1.6–40 billion paired-end reads per run; PE50, PE150, PE250.

Short read

Illumina HiSeq X

1.6–1.8 Tb output, 5.3–6 billion reads per run, 2 × 150 bp.

Short read

Ion Torrent

Fast, targeted next-generation sequencing.

Long read

PacBio & Nanopore

PacBio long reads for genome assembly; Oxford Nanopore PromethION ultra-long reads up to 2 Mb.

Which service do I need?

Your questionSuggested service
What is this bacterium / fungus / fish?Gene-specific (16S, ITS, barcoding)
Does my isolate carry resistance or virulence genes?Whole genome sequencing
Which genes change under my treatment?RNA sequencing
Which microbes live in my soil, water or gut sample?Metagenomics & microbiome
Is DNA methylation different between my groups?Epigenetics
I need primers or probes for PCR.Oligonucleotide synthesis

Ready to start your project?

Tell us your organism, sample type and what you want to find out. We will reply with the right service and a quote.