Sequence the entire genome, including non-coding and intergenic regions. Gives high resolution data for identification and study of genomic variation.
Low cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
nextera normalization library preparation genome illumina WGS dnaMethod for shotgun DNA libraries used for whole genome sequencing and metagenomics.
genome illumina WGS dna tagmentation PCR-free library preparationGold standard method for shotgun DNA libraries used for whole genome sequencing and metagenomics.
WGS dna library preparation truseq genome illuminaLibrary preparation from limited input DNA, used in whole genome sequencing and metagenomics etc.
library preparation truseq genome illumina WGS dnaLibrary preparation for DNA, ideal for preparing libraries from small amounts of input material. Works well for shotgun libraries, ChIP DNA and FFPE samples, amongst others.
WGS dna library preparation genome illuminaNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
assembly long-read nanoporePacBio SMRT sequencing generates reads tens of kilobases in length enabling high quality genome assembly, structural variant analysis, amplicon resequencing, full-length transcript isoform sequencing, full-length 16S rRNA sequencing and amplification free epigenetic characterization.
pacbio methylation amplicon sequel hifi clr de novo iso seq sv smrt assemblyGenotyping-by-sequencing without prior genome information.
polymorphism library preparation genome illumina wholegenome dnaAnalysis applications provided by NGI using PacBio’s open-source SMRT Analysis software suite.
hifi resequencing base modifications pacbio assembly iso-seq structural variation ccs