Design targeted sequencing panels for your regions of interest. Twist Bioscience provides the probes, and NGI handles QC, library prep, and sequencing.
twist bioscience methylation RNA dnaMethod for multiplex protein biomarker analysis (>1000 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink RevealMultiple rounds of barcoding of fixed and permeabilised cells.
transcriptomics RNA mRNA illumina RNA-Seq single-cell parse combinatorialMethod for multiplex protein biomarker analysis (5400 proteins) with sequencing readout using the Illumina NovaSeq platform.
Olink biomarker Olink HT proteinMethod for multiplex protein biomarker analysis with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink ExploreNEBNext EM-Seq kit is an alternative to whole-genome bisulfite sequencing (WGBS). The enzymatic conversion of unmethylated cytosines in EM-seq is more gentle to DNA than WGBS and results in libraries with more even genome coverage and better coverage of CpG sites across the genome.
library preparation methylation epigenetics illumina CpG WGBS EM-seqRNA sequencing of mRNAs selected through poly-A enrichment.
RNA truseq mRNA illumina RNA-Seq library preparation transcriptomicsRNA sequencing of either all RNAs in a sample, or of a RNA sample depleted of for example rRNA by the user.
truseq illumina rnaseq RNA-Seq library preparation RNATotal RNA sequencing based on reduced rRNA content and other type of highly abundant RNAs in both prokaryotic and eukaryotic samples.
library preparation transcriptomics RNA mRNA illumina RNA-SeqNGI offers multiomic spatial profiling through the AVITI24™ with Teton™ CytoProfiling, which combines high-resolution imaging with simultaneous RNA, protein, and morphology detection in a single run.
transcriptomics RNA illumina spatialNGI offers high resolution spatial transcriptomics through the 10x Genomics Visium HD 3’, which combines histology with PolyA-based transcriptomics in HD spatial context
illumina spatial transcriptomics RNAWe now offer high resolution spatially resolved transcriptomics through the 10X Genomics Visium HD CytAssist, which combines histology with probe-based transcriptomics in HD spatial context
transcriptomics RNA illumina spatialWe now offer high resolution spatially resolved transcriptomics through the 10X Genomics Visium HD CytAssist, which combines histology with probe-based transcriptomics in HD spatial context
RNA illumina spatial transcriptomicsWe now offer spatially resolved transcriptomics through the 10X Genomics Visium CytAssist, which combines histology with probe-based transcriptomics in a spatial context.
transcriptomics RNA illumina spatialWe now offer spatially resolved transcriptomics through the 10X Genomics Visium CytAssist, which combines histology with probe-based transcriptomics in a spatial context.
transcriptomics RNA illumina spatialWe offer spatial transcriptomics through the 10X Genomics Visium method. The method combines histology with unbiased transcriptomics in a spatial context.
transcriptomics RNA illumina spatialA method to identify open chromatin regions, such as promotor areas, using a transposase.
Omni-ATAC TN5 ATAC open chromatin epigenetics illumina ATACseq ATAC-seqCombining short & long reads at the single cell level.
long-read illumina ont chromium 10x Genomics full transcript library preparation single cellProfiling of chromatin accessibility at the single cell level.
illumina ATAC-seq dna chromium chromatin 10x Genomics ATAC library preparation epigenetics single cellProfiling of 3´gene expression and chromatin accessibility in the same cell.
ATAC chromium library preparation 10x Genomics transcriptomics single cell RNA mRNA illumina ATAC-seq RNA-SeqProfiling of gene expression levels at single-cell resolution.
RNA mRNA illumina RNA-Seq chromium 10x Genomics library preparation transcriptomics single cellSingle-cell profiling of gene expression levels on fixed cells/nuclei.
transcriptomics single cell multiplexing RNA probes mRNA FFPE illumina RNA-Seq sequencing chromium 10x Genomics library preparation fixed cellsA proximity-ligation protocol using a sequence-independent endonuclease, generating data for TAD identification and scaffolding.
chromatin scaffolding library preparation epigenetics TADs illumina de novoNGI now offers High Molecular Weight (HMW) DNA extraction as a service for sequencing projects at or in collaboration with NGI and SciLifeLab.
dna extraction hmw hmw dnaSequencing of the 16S gene to study bacterial diversity and composition in a sample.
amplicon targeted library preparation illumina 16SSequencing of PCR amplicons to study genetic variation within small target regions.
library preparation illumina 16S amplicon targetedG-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.
illumina WGS dna single-stranded DNA ssDNA library preparation genomeSPLAT is an in-house developed WGBS library preparation method. This approach enables quick and efficient preparation of WGBS libraries from low-input DNA
ssDNA library preparation methylation epigenetics illumina CpG WGBS Bisulphite single-stranded DNALow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
normalization library preparation genome illumina WGS dna nexteraNGI 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.
illuminaMethod 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.
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 cDNA sequencing is able to sequence entire transcripts in one go, ideal for detecting isoforms and fusions events.
assembly long-read nanoporeNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
long-read nanopore assemblyNanopore direct RNA sequencing is able to sequence entire transcripts from native RNA, opening up opportunities to detect RNA 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.
smrt assembly pacbio methylation amplicon hifi de novo iso seq sv revioGenotyping-by-sequencing without prior genome information.
library preparation genome illumina wholegenome dna polymorphismA platform for human whole exome sequencing (WES) using target enrichment and library preparation for next generation sequencing.
library preparation illumina dna exome targetedWe offer a broad range of microarray options for high-throughput genotyping solutions based on SNP complexity and organism.
illumina genotyping dna array infinium SNPThe EPIC BeadChip array allows for the interrogation over 935,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
array infinium CpG methylation epigenetics illumina dna