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Genomic DNA Sample Prep Kits
Sample Prep Workflow
Genomic DNA Sample Prep Kits
| System: | Genome Analyzer, iScanSQ |
|---|---|
| Technology: | Illumina Sequencing |
| Assay: | Single-Read Sequencing |
| Applications: | DNA Sequencing, Cytogenetic Analysis, DNA-Protein Interaction Analysis (ChIP-Seq), Small RNA Discovery and Analysis |
| Contents: | Reagents for library preparation of 10-40 DNA samples; Oligo only kit contains adapters and PCR primers to prepare 100 DNA samples |
The Genomic Sample Prep Kit is used to build DNA libraries for single-read sequencing. Random size-selected DNA fragments are generated and prepared for addition of unique adapters. Following a short PCR enrichment, the library is ready to load on cBot for cluster generation.
Applications
Sequencing
Illumina sequencing gives you the power to comprehensively characterize the genome, epigenome or the transcriptome. Go from DNA to data in under a week with less than four hours of hands-on time. Applications flexibility for any genetic variant. Superior raw-read accuracy and the industry’s simplest, automated workflow. It’s sequencing power for every researcher.
More...SNP Genotyping and CNV Analysis
A diverse range of genotyping solutions allow you to investigate genetic variation on any scale, from customized studies on specific regions of interest to large-scale genome-wide association studies. With proven assays, the most advanced genomic content, and robust array platforms, generate the highest quality data and best reproducibility in the industry.
More...Gene Regulation and Epigenetic Analysis
Illumina offers a range of powerful solutions for analyzing epigenetic and gene regulation events such as CpG methylation, histone modifications, or DNA-protein interactions. With next-generation sequencing, you can view the epigenome at single-base resolution to unlock to every detail hidden within. Our array-based assays provide high-throughput, quantitative measurement of CpG methylation at the single-site level, offering outstanding resolution for methylation profiling studies.
More...Cytogenetics
Illumina’s cytogenetic analysis solutions give you the ability to rapidly discover and profile structural aberrations across the genome. Our microarray-based assays allow you to screen against all known cytogenetic abnormalities and discover new regions. With next-generation sequencing, combine short-insert and long-insert paired-end reads to catalog any size genomic rearrangement and evaluate complex aberrations.
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