High-throughput full-genome or targeted sequencing of DNA from organisms with an existing reference genome.
Adaptive sampling is an Oxford Nanopore Technologies (ONT) method for real-time targeted sequencing. The method enables enrichment or depletion of specific genomic regions during sequencing without additional library preparation steps.
adaptive sampling nanoporeCost-efficient, high-throughput library preparation for whole-genome sequencing of large sample collections. Only for sample batches of 96.
library preparation genome WGS dna affordableFlexible whole genome library preparation with PCR-free workflows from as little as 100 ng DNA and PCR workflows for lower-input samples.
Design targeted sequencing panels for your regions of interest. Twist Bioscience provides the probes, and NGI handles QC, library prep, and sequencing.
methylation RNA dna twist bioscienceFull length sequencing of the 16S gene provides a significantly higher taxonomic resolution compared to sequencing of isolated regions.
library preparation illumina 16S amplicon targetedSequencing of the 16S V3/V4 region to study bacterial diversity and composition in a sample.
targeted library preparation illumina 16S ampliconSequencing of PCR amplicons to study genetic variation within small target regions.
illumina 16S amplicon targeted library preparationG-SPLAT is a library preparation technique designed for low-quality or limited-input DNA, with applications in whole-genome sequencing, metagenomics, and and other challenging sequencing projects.
ssDNA library preparation genome illumina WGS dna single-stranded DNALow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
illumina WGS dna nextera normalization library preparation genomeMethod for shotgun DNA libraries used for whole genome sequencing and metagenomics.
dna tagmentation PCR-free library preparation genome illumina WGSGold standard method for shotgun DNA libraries used for whole genome sequencing and metagenomics.
genome illumina WGS dna library preparation truseqLibrary preparation from limited input DNA, used in whole genome sequencing and metagenomics etc.
genome illumina WGS dna library preparation truseqLibrary 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.
genome illumina WGS dna library preparationNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
long-read nanopore assemblyPacBio 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.
revio smrt assembly pacbio methylation amplicon hifi de novo iso seq svGenotyping-by-sequencing without prior genome information.
genome illumina wholegenome dna polymorphism library preparationA platform for human whole exome sequencing (WES) using target enrichment and library preparation for next generation sequencing.
exome targeted library preparation illumina dnaQuality control, Basecalling and multiplexing of sequencing reads generated by Oxford Nanopore sequencers.
long-read nanoporeAdditional compute intensive nanopore raw data processing services provided by NGI
methylation base modifications basecalling pod5Basic quality-control monitoring of Illumina FastQ sequence data.
QC fastqc fastq screen checkqcRuns with illumina DNA-sequencing data, WGS or targeted sequencing e.g. WES. Aligns to the reference genome, gives QC metrics, does variant-calling and finishes with annotation.
sarek cancer human data WES WGS