NGI can sequence libraries prepared by research groups.
NGI can sequence user-prepared libraries on the Aviti platform. User-prepared libraries orders can only be sequenced on whole flowcells.
illumina avitiNGI can sequence user-prepared libraries on all Illumina instruments. User-prepared libraries orders can only be whole-lane orders. Libraries with custom setups and or custom primers can only be whole flow cells.
illuminaNGI can sequence user-prepared libraries on Oxford Nanopore PromethION. User-prepared libraries orders can only be sequenced on whole flowcells.
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.
smrt assembly pacbio methylation amplicon hifi de novo iso seq sv revioAdditional compute intensive nanopore raw data processing services provided by NGI
base modifications basecalling pod5 methylationBasic quality-control monitoring of Illumina FastQ sequence data.
QC fastqc fastq screen checkqc