nextRAD services

nextRAD genotyping by sequencing samples a genome at thousands of loci across the genome. Each locus is sequenced with 122 bp reads and these reads are compared between samples to identify SNPs. A reference genome is not required for nextRAD genotyping.

Project pricing includes quality check of genomic DNA, creation of nextRAD libraries, sequencing, and bioinformatics (creation of genotype table). Extra charges apply for genome sizes greater than 1 gigabase.



95 samples

190 samples

380 samples

  7,000   loci 

single-end 122 bp reads at an average 20X read depth

not available

$55/sample

$50/sample

15,000 loci

single-end 122 bp reads at an average 20X read depth

$69/sample

$66/sample

$61/sample

30,000 loci

single-end 122 bp reads at an average 20X read depth

$84/sample

$81/sample

$76/sample