Targeted Sequencing
Targeted sequencing is a technique that uses NGS to target specific genes, coding regions of the genome, or chromosomal segments for rapid identification and analysis of genetic mutations.
High-Throughput Genotyping | CRISPR Validation
High-throughput genotyping is a next generation sequencing (NGS) assay ideal for ultra-sensitive, high-throughput, sample-to-answer genotyping projects, enabling validation of targeted CRISPR gene editing experiments.
Whole Genome Sequencing
Whole genome sequencing (WGS) is the comprehensive read and analysis of an entire genome, including non-coding regions of the genome.
Amplicon Sequencing
Amplicon sequencing is a targeted sequencing method that uses polymerase chain reaction (PCR) to selectively amplify specific DNA fragments or genomic regions of interest.
Whole Exome Sequencing
Whole exome sequencing is a powerful tool to investigate genetic variations underlying cancers, Mendelian diseases, and complex human disorders.
Single Cell Sequencing
Single-cell sequencing provides transcriptional profiling of thousands of individual cells.
High Throughput Gene Expression Screening
High-throughput gene expression (HT-GEx) screening is an optimal approach for drug discovery and analysis, similar to DRUG-Seq.
Next Generation Sequencing Sample Submission Guidelines
Next Generation Sequencing is a technology in which nucleotides are added in parallel to the copying of a DNA strand. When nucleotides are incorporated into the growing DNA strand, a signal is generated that corresponds to the nucleotide type and position. GENEWIZ Next generation sequencing services offer both standard and custom options for extraction, library preparation, sequencing, and bioinformatics.
RNA Sequencing | RNA-Seq
RNA sequencing (RNA-Seq) is a highly effective method for studying the transcriptome qualitatively and quantitatively. It can identify the full catalog of transcripts, precisely define gene structures, and accurately measure gene expression levels.
Next Generation Sequencing (NGS)
Next Generation Sequencing is a technology in which nucleotides are added in parallel to the copying of a DNA strand. When nucleotides are incorporated into the growing DNA strand, a signal is generated that corresponds to the nucleotide type and position. GENEWIZ Next generation sequencing services offer both standard and custom options for extraction, library preparation, sequencing, and bioinformatics.