NEBNext 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.
illumina CpG WGBS EM-seq library preparation methylation epigeneticsThe complexity and polymorphic nature of the 4 Mb region makes it challenging to resolve using short-read sequencing technology. Nanopore (ONT) sequencing, can provide long reads that overcome these challenges, enabling the identification of variants that could represent new biomarkers, unambiguous haplotype phasing of single-nucleotide variants (SNVs), and the potential for increased accuracy of HLA typing at a higher resolution.
library preparation nanoporeMethod for multiplex protein biomarker analysis with sequencing readout using the Illumina NovaSeq platform.
Olink Explore protein Olink biomarkerMethod for multiplex protein biomarker analysis (5400 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink HTMethod for multiplex protein biomarker analysis (>1000 proteins) with sequencing readout using the Illumina NovaSeq platform.
protein Olink biomarker Olink RevealProfiling of gene expression levels at single-cell resolution.
transcriptomics single cell illumina rnaseq smartseq3 SS3 single-cell library preparationRNA sequencing of mRNAs selected through poly-A enrichment.
RNA-Seq library preparation transcriptomics RNA truseq mRNA illuminaRNA sequencing of either all RNAs in a sample, or of a RNA sample depleted of for example rRNA by the user.
RNA-Seq library preparation RNA truseq illumina rnaseqTotal RNA sequencing based on reduced rRNA content and other type of highly abundant RNAs in both prokaryotic and eukaryotic samples.
RNA mRNA illumina RNA-Seq library preparation 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.
illumina spatial transcriptomics RNAWe offer spatial transcriptomics through the 10X Genomics Visium method. The method combines histology with unbiased transcriptomics in a 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
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 spatialA method to identify open chromatin regions, such as promotor areas, using a transposase.
ATAC open chromatin epigenetics illumina ATACseq ATAC-seq Omni-ATAC TN5Single-cell profiling of gene expression levels on a large number of cells.
mRNA illumina RNA-Seq scale library preparation transcriptomics single cell RNASingle-cell profiling of gene expression levels on fixed cells.
RNA mRNA illumina RNA-Seq chromium 10x Genomics fixed cells library preparation transcriptomics single cellProfiling of chromatin accessibility at the single cell level.
library preparation epigenetics single cell illumina ATAC-seq dna chromium chromatin 10x Genomics ATACProfiling of 3´gene expression and chromatin accessibility in the same cell.
illumina ATAC-seq RNA-Seq ATAC chromium library preparation 10x Genomics transcriptomics single cell RNA mRNAProfiling of gene expression levels at single-cell resolution.
library preparation transcriptomics single cell RNA mRNA illumina RNA-Seq chromium 10x GenomicsCombining short & long reads at the single cell level.
library preparation single cell long-read illumina ont chromium 10x Genomics full transcriptA proximity-ligation protocol using a sequence-independent endonuclease, generating data for TAD identification and scaffolding.
TADs illumina de novo chromatin scaffolding library preparation epigeneticsNGI 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.
library preparation illumina 16S amplicon targetedSequencing of PCR amplicons to study genetic variation within small target regions.
illumina 16S amplicon targeted library preparationSPLAT is an in-house developed WGBS library preparation method. This approach enables quick and efficient preparation of WGBS libraries from low-input DNA
methylation epigenetics illumina CpG WGBS Bisulphite single-stranded DNA ssDNA library preparationLow cost library preparation option for gDNA based on bead-linked transposase. Only for full plates of samples.
illumina WGS dna nextera normalization library preparation genomeNGI 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.
dna library preparation truseq genome illumina WGSLibrary 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.
illumina WGS dna library preparation genomeNanopore cDNA sequencing is able to sequence entire transcripts in one go, ideal for detecting isoforms and fusions events.
long-read nanopore assemblyNanopore instruments can sequence very long continuous fragments of DNA. Sequencing native DNA allows detection of base modifications.
assembly long-read nanoporeNanopore direct RNA sequencing is able to sequence entire transcripts from native RNA, opening up opportunities to detect RNA 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.
methylation amplicon hifi de novo iso seq sv revio smrt assembly pacbiomiRNA libraries from very low input total RNA samples & degraded total RNA.
illumina library preparation epigenetics RNAGenotyping-by-sequencing without prior genome information.
genome illumina wholegenome dna polymorphism library preparationThe Takara SMARTer Stranded Total RNA-Seq Kit v3 - Pico Input Mammalian kit is specifically designed for very low input total RNA samples. It also works with degraded total RNA.
illumina rnaseq RNA-Seq depletion library preparation transcriptomics RNAA 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.
array infinium SNP illumina genotyping dnaThe EPIC BeadChip array allows for the interrogation over 935,000 methylation sites quantitatively across the genome at single-nucleotide resolution.
methylation epigenetics illumina dna array infinium CpG