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Highly Scalable
Submit one to hundreds of samples
Flexible Data Amounts
Starting at 10M paired end reads
Latest Platforms
Illumina® NovaSeq™ delivers the highest throughput
European Provider
Sequencing available at our lab in Leipzig, Germany
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Next Generation Sequencing
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Sequencing OnlyRNA-SeqSingle-Cell RNA SequencingExome SequencingAmplicon Sequencing ServicesCRISPR ValidationTargeted Reseq & Custom Gene PanelsMetagenomics SolutionsEpigenomicsImmunogenomics
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Sanger Sequencing
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Service & OptionsBarcodes for Sanger SequencingLogistic Options
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Gene Synthesis
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Standard Gene Synthesis (PriorityGENE)TurboGENE™FragmentGENESynthetic DNA LibrariesCRISPR Construct SynthesisssDNA Synthesis NewDNA CloningSite-Directed Mutagenesis
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Molecular Genetics
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Bacterial and Fungal IdentificationMutation AnalysisSNP GenotypingPCR Plus Sequencing CRISPR Analysis PackagecDNA & gDNA Verification ServicesYeast Colony SequencingFragment Analysis
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Plasmid DNA Preparation
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Standard Plasmid DNA PreparationTargeted Yield Plasmid DNA Preparation
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Oligo Synthesis Services
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Oligo-Rapid SynthesisOligo-Flex SynthesisOligo Retained for Sanger Sequencing
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GLP-Compliant Services
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Confirmatory SequencingSNP Mutation Analysis
Plasmid Prep
Nucleic Acid Extraction
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Clinical Services NEW
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CLIA Variant Confirmation (PCR + Sanger)CLIA Sanger SequencingCLIA Whole Exome SequencingCLIA Whole Genome Sequencing
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RNA SEQUENCING
RNA sequencing (RNA-Seq) is a powerful method for studying the transcriptome qualitatively and quantitatively. It can identify the full catalog of transcripts, precisely define the structure of genes, and accurately measure gene expression levels.
GENEWIZ provides unparalleled flexibility in the analysis of different RNA species (coding, non-coding, and small transcripts) from a wide range of starting material using long- or short-read sequencing.
RNA Sequencing Services
Single-Cell RNA-Seq
Single-cell RNA sequencing analyzes gene expression at single-cell resolution for heterogeneous samples. The 10x Genomics® Chromium™ platform provides advanced transcriptional profiling of thousands of individual cells.
Standard RNA-Seq
Standard RNA sequencing is our most popular option for profiling gene expression, enabling the analysis of coding (mRNA) and long non-coding RNA (lncRNA).
Strand-Specific RNA-Seq
Strand-specific RNA sequencing provides gene expression information with relation to strand orientation. Used for genome annotation, analysis of anti-sense/overlapping transcripts, and novel transcript discovery.
Small RNA-Seq
Small RNA sequencing enables analysis of miRNA and other small RNA species. Provides small RNA discovery and profiling.
Features & Benefits
Superior data quality with a guarantee of ≥80% bases with ≥Q30 for 2x150 bp sequencing (>90% on average)
Industry-leading turnaround time as fast as 1 week
Dedicated support from Ph.D.-level project managers at every step including post-delivery support
Complete sample-to-analysis solutions including flexible extraction and data analysis options available
Tech Note: Add More Life to Your Data: Optimizing Single-Cell RNA-Seq with Dead Cell Removal
Obtaining samples with high cell viability can be difficult for many experiments but is necessary for success on the 10x Genomics® Chromium™ platform. This tech note describes how GENEWIZ scientists used optimized single-cell workflows, including dead cell removal, to overcome low viability and generate high-quality sequencing data.
Case Study: Uncovering Cell Type-Specific Expression Profiles in the Tumor Microenvironment with Ultra-Low Input RNA-Seq
Biomedical specimens are often restricted to minute quantities, posing major limitations to RNA-Seq. This case study shows how approximately 50 sorted cells from a glioblastoma can produce transcriptomic data comparable to RNA-Seq experiments that use millions of cells.
Case Study: Single-Cell RNA-Seq Analysis Identifies Rare Drug-Resistant Cancer Stem Cells
Cell populations are rarely homogeneous and synchronized in their characteristics. Standard RNA-Seq approaches are limited to reporting general expression levels thus omitting minor subpopulation profiles. This study highlights new single-cell RNA sequencing capabilities for identifying rare cells, characterizing their transcriptomes, and discovering potential biomarkers.
Tech Note: Isoform Sequencing on the PacBio Sequel® – Maximizing Output and Accuracy
Contiguous mRNA full-length sequencing (Iso-Seq) greatly simplifies genome annotation efforts and revolutionizes the discovery of novel RNA isoforms. This Tech Note discusses the advantages of the latest technologies combined with GENEWIZ’s optimized workflow, and how this increases output and accuracy.
NGS PLATFORMS
ILLUMINA® NOVASEQ™/HISEQ®
PACBIO® SEQUEL®
10X GENOMICS® CHROMIUM™
