Illumina HiScanSQ

HiScanSQ


应用: DNA测序, 基因调控分析, 测序法转录组分析, SNP发现和结构变异分析, 定制基因分型, 细胞遗传学分析, 连锁分析, 全基因组基因分型和拷贝数分析, DNA-蛋白相互作用分析（ChIP-Seq）, 测序法甲基化分析, 小RNA发现和分析, 阵列法甲基化分析, 定制低至中多重甲基化分析, 阵列法转录组分析, FFPE样品分析, 全基因组基因表达分析, 定制低至中多重基因表达分析


HiScanSQ整合了基因分型、基因表达和甲基化阵列的高通量性能，以及新一代测序的力量和分辨率，为实验设计带来了前所未有的灵活性。更多信息...


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系统描述

仪器特有两个不同的组件：HiScan Reader——一台高性能的扫描仪，以及SQ Module——一个附加的流体学设备，能够实现基因组规模的测序。HiScan Reader作为一台适用于Illumina BeadArray产品的高速精确的芯片扫描仪，独立地发挥作用。有了SQ Module，系统迅速地转换到执行Illumina的边合成边测序技术，即世界上最广泛采用的新一代测序技术。

芯片和测序技术的相互促进，为遗传学发现和验证提供了一种有力的方法，实现了广泛的应用，具有无限探索的潜能。

  

优势

为灵活性而设计

将芯片的高通量处理与新一代测序的力量和分辨率相结合。

久经考验的性能

享用目前最成功、最值得信赖的阵列和测序技术。

一种简化的方案

通过多个前沿的用户界面让仪器手工操作时间最小化，特有自动化且简化的实验设置和处理步骤。

 

 

两种久经考验的技术，一个强大的平台

HiScanSQ整合了久经考验的 阵列 和 测序 技术，这两项技术催生了性状和疾病研究方面大量开创性的发现。利用您所信赖的技术和以您的方式设计的实验，询问基因组、转录组和表观基因组方面的任何问题。

 

会议消息

European Society of Human Genetics (ESHG)
June 12-15, 2010
Gothenburg, Sweden

流程 & 规格


HiScanSQ Specifications

流程

简化的芯片和测序流程让您能快速生成高质量数据，既方便又可靠。


分析/方案

BeadArray: Infinium HD, Infinium 甲基化, DASL, 直接杂交, GoldenGate 基因分型
测序: 单读测序, 对读测序, 多重测序, 配对末端文库测序, ChIP-Seq 测序, mRNA-Seq, 小RNA发现和分析, MicroRNA 测序, 对读测序, 蛋白核酸相互作用


HiScan Reader的物理规格
宽 28.3 in (71.9 cm)
高 30.1 in (76.5 cm)
深 27.5 in (69.9 cm)
重 300 lbs (136 kg)
SQ Module的物理规格
宽 23.1 in (58.7 cm)
高 29.1 in (73.9 cm)
深 23.2 in (58.9 cm)
重 194 lbs (84.5 kg)
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HiScanSQ Kits

AutoLoader 2.x

AutoLoader 2.x

For faster genome analysis the AutoLoader 2.x has walk-away BeadChip loading and scanning for the iScan and HiScanSQ Systems. With continuous unattended operation, and the ability to load one or two microarray Readers, the AutoLoader 2.x improves assay efficiency and decreases costs. With two input and two output stacks up to 80 BeadChips can be handled unattended.

Additional Details

SY-202-1001
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MaizeSNP50 DNA Analysis Kits

MaizeSNP50 DNA Analysis Kits

The Maize SNP50 DNA Analysis BeadChip enables the interrogation of genetic variation across maize lines. Illumina has developed this BeadChip in collaboration with TraitGenetics, The French National Institute for Agricultural Research (INRA), and Syngenta. This BeadChip contains more than 50,000 validated markers derived from the B73 reference sequence. Importantly, this BeadChip presents an average of greater than 25 markers per megabase (Mb), providing ample SNP density for robust whole-genome genotyping studies.

Additional Details

WG-500-1001
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African American Admixture Panel

African American Admixture Panel

The African American Admixture Panel facilitates detection of susceptibility loci of genetic variants that differ in frequency between ancestral African and European populations. Regions with African ancestry deviating from average may contain genetic variants associated with disease. The panel contains 1,509 SNPs for admixture mapping studies.

Additional Details

GT-17-230
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Bovine SNP50 DNA Analysis Kits

Bovine SNP50 DNA Analysis Kits

The Bovine SNP50 DNA Analysis BeadChip contains 54,609 highly informative SNPs uniformly distributed across the entire genome of major cattle breed types. This empowers applications such as genome-wide enabled selection, identification of quantitative trait loci, evaluation of genetic merit of individuals, and comparative genetic studies.

Additional Details

WG-450-2001
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HumanCytoSNP-12 DNA Analysis BeadChip Kits

HumanCytoSNP-12 DNA Analysis BeadChip Kits

The 12-sample HumanCytoSNP-12 BeadChip is a powerful, whole-genome scanning panel for efficient, high-throughput analysis of genetic and structural variations relevant to human disease. Many variations in the human genome that affect phenotypes can be detected including duplications, deletions, amplifications, copy-neutral LOH, and mosaicism.

Additional Details

WG-320-2101
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Human1M-Duo DNA Analysis BeadChip Kits

Human1M-Duo DNA Analysis BeadChip Kits

The Human1M-Duo DNA Analysis BeadChip interrogates 1.2 million loci per sample, with genome-wide coverage of SNPs. Content is focused on tag SNPs, SNPs in genes, and SNPs and non-polymorphic markers in known and novel CNV regions. Simultaneous processing of two samples increases sample throughput and decreases experimental variability.

Additional Details

WG-311-1105
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Cancer SNP Panel

Cancer SNP Panel

Illumina's Cancer SNP Panel provides tools for conducting candidate-gene based association studies. The Panel consists of 1,421 thoroughly screened and validated SNP loci from > 400 genes thought to be involved in cancer. Panel content was selected from the National Cancer Institute’s Cancer Genome Anatomy Project SNP500 Cancer Database.

Additional Details

GT-17-211
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Canine SNP20 DNA Analysis Kits

Canine SNP20 DNA Analysis Kits

The Canine SNP20 DNA Analysis BeadChip offers a solution for genome-wide association studies within domestic dog breeds. Illumina has developed this BeadChip with Broad Institute researchers, who first completed the assembly of the canine genome, CanFam2.02. This BeadChip contains 22,362 validated SNP probes derived from the CanFam2.0 assembly.

Additional Details

WG-31-123
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CanineHD Whole-Genome Genotyping Kits

CanineHD Whole-Genome Genotyping Kits

Featuring highly polymorphic SNP content and providing uniform genomic coverage (Figure 2), the CanineHD BeadChip enables the interrogation of genetic variation in any domestic dog breed. Importantly, this BeadChip presents an average of greater than 70 markers per megabase (Mb), providing ample SNP density for robust within-breed association and copy number variation (CNV) studies.

Additional Details

WG-440-1001
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Custom GoldenGate Panels (OPAs)

Custom GoldenGate Panels (OPAs)

Illumina Custom GoldenGate Genotyping Panels allow researchers to create assays tailored directly to their specific needs for targeted region genotyping or fine-mapping of candidate disease association regions. GoldenGate Custom Panels provide flexibility and high data quality across a wide range of genomes and experimental designs.

Additional Details

GT-17-110
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DNA Activation Kits

DNA Activation Kits

DNA Activation Kits are used in the first steps of the GoldenGate protocol to make biotin-labeled DNA that is then purified for use in the GoldenGate Assay amplification step. The DNA sample used in this assay is activated for binding to paramagnetic particles. This activation step requires a minimum input of DNA (250ng at 50ng/μl).

Additional Details

GT-95-201
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DNA Test Panel

DNA Test Panel

Illumina's DNA Test Panel is a SNP-based tool for pre-screening DNA samples for assay performance before conducting studies with larger numbers of loci. The Panel consists of 360 SNP loci distributed across the genome, chosen from the LinkageIVb Panel. DNA Test Panel loci were designed as genomic controls not likely to be associated with disease.

Additional Details

GT-17-221
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Equine SNP50 DNA Analysis Kits

Equine SNP50 DNA Analysis Kits

The Equine SNP50 DNA Analysis BeadChip features 54,602 SNPs uniformly distributed across the entire genomes of 15 horse breeds. Content is derived from the EquCab2.0 SNP collection compiled by the Broad Institute’s Equine Genome Sequencing Project. This BeadChip enables horse researchers to conduct a broad range of genome-wide geno­typing studies.

Additional Details

WG-402-1001
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GoldenGate Assay Kits

GoldenGate Assay Kits

GoldenGate Assay Kits provide the reagents for the core of the DASL Gene Expression protocol, including extension, ligation, clean up, and hybridization to the multi-sample array format of choice.

Additional Details

DA-95-203
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GoldenGate Genotyping Kits

GoldenGate Genotyping Kits

GoldenGate Genotyping Kits provide reagents for the GoldenGate Genotyping Assay, including extension, ligation, cleanup, and hybridization to the multi-sample array format of choice. The kits are available with or without Uracil DNA Glycosylase. The Assay allows for a high degree of loci multiplexing during extension and amplification steps.

Additional Details

GT-95-203
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GoldenGate Indexing v1 Kit

GoldenGate Indexing v1 Kit

GoldenGate Indexing is a high-throughput genotyping solution that combines multi-sample indexing technology within the proven GoldenGate assay with automation control and positive sample tracking through an Illumina Laboratory Information Management System (LIMS). The GoldenGate Indexing assay is conveniently processed on the Universal-32 BeadChip.

Additional Details

GT-222-1003
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HumanCVD Whole-Genome Genotyping Kits

HumanCVD Whole-Genome Genotyping Kits

The HumanCVD BeadChip is a high-density SNP genotyping standard panel specifically targeted for cardiovascular disease studies (CVD). The BeadChip features nearly 50,000 markers that capture genetic diversity across approximately 2,100 genes The HumanCVD BeadChip is a multi-sample genotyping panel powered by Illumina’s Infinium II Assay.

Additional Details

WG-31-151
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HumanLinkage V Panel Set

HumanLinkage V Panel Set

The HumanLinkage V Panel Set is optimized to detect recombination events. Linkage analysis is a powerful approach for mapping the location of disease-causing loci. The likelihood of a recombination event occurring between two markers is related to the distance between them. Markers closest to a disease gene will co-segregate most strongly with the disease phenotype.

Additional Details

GT-17-240
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Infinium iSelect HD Custom Genotyping BeadChip

Infinium iSelect HD Custom Genotyping BeadChip

Infinium iSelect HD Custom Genotyping offers access to the entire genome, and custom Infinium content, including non-human species. Custom Genotyping allows the design of a panel from 3,000-200,000 attempted bead types on a 12-sample (60,801 to 200,00) or 24-sample (3,000 to 60,800) BeadChip format. Assay virtually any genome marker, disease or pathway specific markers, rare variants, CNVs, and more.

Additional Details

WG-35-101
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MHC Exon-Centric Panel

MHC Exon-Centric Panel

The MHC region contains genomic sequences that contribute to autoimmune and inflammatory disorders. The MHC Exon-Centric Panel employs an approach for association mapping genetic regions of interest that focuses on SNPs near and within coding exons. Exploration of this region can help determine gene associations that lead to disease susceptibility.

Additional Details

GT-17-191
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MHC Mapping Panel

MHC Mapping Panel

The MHC Mapping Panel can be used to map variants in the MHC region. This region is proposed to contain genomic sequences that contribute to the majority of autoimmune and inflammatory disorders. Exploration of this region can provide information to determine the gene associations that lead to disease susceptibility.

Additional Details

GT-17-181
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MHC Panel Set

MHC Panel Set

Illumina’s Major Histocompatibility Complex (MHC) Panel Set consists of two assay pools of oligonucleotides: the MHC Mapping Panel and the MHC Exon-Centric Panel. These panels provide a mapping of disease-associated variants. The MHC region contains genomic sequences that contribute to the majority of autoimmune and inflammatory disorders.

Additional Details

GT-17-171
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Mouse MD Linkage

Mouse MD Linkage

Illumina’s Mouse MD Linkage Panel consists of SNP loci that have been selected from the Wellcome-CTC Mouse Strain SNP Genotype Set. The Panel consists of 1,449 loci and is optimal for various mapping applications that include characterization of transgenic, congenic and knockout animals, and genetic mapping in advanced intercross mouse lines.

Additional Details

GT-18-131
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Mouse LD Linkage

Mouse LD Linkage

The mouse has been increasingly recognized as an optimal genetic system for the study of the genetics of complex disease traits. The Mouse LD Linkage Panel is a SNP panel that offers a low-cost, efficient method for attaining genome-wide genetic data to identify quantitative trait loci, map candidate genes, and increase genotyping throughput.

Additional Details

GT-18-121
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OvineSNP50 DNA Analysis Kits

OvineSNP50 DNA Analysis Kits

The OvineSNP50 BeadChip features over 54,241 evenly spaced probes that target SNPs. This BeadChip offers more than sufficient SNP density for genome-wide association studies and other applications such as genome-wide selection, determination of genetic merit, identification of quantitative trait loci, and comparative genetic studies.

Additional Details

WG-420-1001
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PorcineSNP60 DNA Analysis Kits

PorcineSNP60 DNA Analysis Kits

The PorcineSNP60 DNA Analysis BeadChip features 62,163 evenly spaced probes offering more than sufficient SNP density for whole-genome association studies and other applications. This 12-sample BeadChip presents a superior solution for interrogating genetic variation in multiple porcine breeds, including Duroc, Landrace, Pietran, and Large White.

Additional Details

WG-410-1001
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Universal Arrays

Universal Arrays

GoldenGate Assays are deployed on the 12- or 32-sample Universal BeadChips or 96-sample Universal Array Matrix during the GoldenGate Genotyping Assay hybridization step. They contain universal sequences that hybridize to complementary sequences in the prepared sample. Both make use of the high density self-assembly of oligonucleotide-coated beads.

Additional Details

GT-221-1003
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cDNA Synthesis Kits

cDNA Synthesis Kits

cDNA Synthesis Kits are used in the first step of the DASL Assay protocol where total RNA is converted to cDNA using both biotinylated nonamers (biotin-d(N)9) and biotinylated oligo d(T)18 that is then cleaned up and ready for use in the GoldenGate Assay amplification step.

Additional Details

DA-95-501
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Custom DASL Panels (DAPs)

Custom DASL Panels (DAPs)

Custom DASL Assay Panels (DAPs) can be generated for between 512-1536 genes. Design is a collaborative process. Oligo probes for standard expression panels and custom sets are subjected to bioinformatics screening that assesses each target site for specificity in transcriptome and genome, and also assesses predicted behavior in DASL biochemistry.

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This product is currently unavailable.
Custom Oligo Pool for Methylation Assay (OMA)

Custom Oligo Pool for Methylation Assay (OMA)

The Custom Oligo Pool for Methylation Assay (OMA) provides flexibility and high data quality across a wide range of genomes and experimental designs. Customers can select assays to target CpG loci within specific genes or regions of interest. Custom Oligo Pools are available for 384 to 1,536 CpG sites in multiples of 96.

Additional Details

GM-17-110
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DASL Human Cancer Panel

DASL Human Cancer Panel

The DASL Human Cancer Panel is a pool of selected probe groups that targets 502 genes collected from ten publicly available cancer gene lists. Genes were chosen based on frequency of appearance and frequency of literature citations association with cancer. Each gene in the Cancer Panel is targeted in three locations with three probe sets per gene.

Additional Details

DA-10-100
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DASL Universal Arrays

DASL Universal Arrays

DASL Universal Arrays include the 96-sample DASL Universal Array Matrix and the 16-sample DASL Universal BeadChip formats. Instead of gene-specific sequences, Universal Arrays contain universal sequences, or addresses, that hybridize to complementary sequences in the prepared sample.

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This product is currently unavailable.
Goldengate Methylation Assay and Beadchip Kit

Goldengate Methylation Assay and Beadchip Kit

The GoldenGate Methylation Assay and BeadChip Kit provides reagents for extension, ligation, clean up, and hybridization to the multi-sample array format of choice for analysis in the GoldenGate Methylation Assay.

Additional Details

GM-904-0204
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GoldenGate Methylation Assay Kits

GoldenGate Methylation Assay Kits

GoldenGate Methylation Assay Kits provide reagents for extension, ligation, clean up, and hybridization to the multi-sample array format of choice. GoldenGate Methylation Kits consist of three boxes of reagents, available with or without Uracil DNA Glycosylase (UDG). UDG is recommended as a contamination prevention mechanism.

Additional Details

GM-95-203
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GoldenGate Methylation DNA Activation Kit

GoldenGate Methylation DNA Activation Kit

GoldenGate Methylation DNA Activation Kits are used in the first steps of the GoldenGate Methylation protocol to make biotin-labeled DNA that is then purified and ready for use in the GoldenGate Methylation Assay amplification step.

Additional Details

GM-95-201
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Infinium HumanMethylation27, RevB BeadChip Kits

Infinium HumanMethylation27, RevB BeadChip Kits

The HumanMethylation27 BeadChip is a solution for surveying genome-wide DNA methylation profiles. The BeadChip allows interrogation of 27,578 CpG highly informative sites per sample at single-nucleotide resolution. Using the Infinium Assay Illumina scientists created a panel of high-value methylation sites, including promoters and hotspots.

Additional Details

WG-311-2201
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Methylation Universal Arrays

Methylation Universal Arrays

The 96-sample Universal Array Matrix (SAM) is used in the hybridization step of the GoldenGate Methylation Assay, which combines high sample throughput, high multiplexing, and single-site CpG resolution. The Universal Array contains universal sequences or addressed that hybridize to complementary sequences in the prepared sample.

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GM-103-1203
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Multi-Format GEX Buffer Kit

Multi-Format GEX Buffer Kit

Buffer set for use with Expression BeadChips with low-volume seals. Includes sufficient hybridization buffer, wash buffer, and trays to process six BeadChips

Additional Details

BD-20-104
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HumanHT-12 v3 Expression BeadChip Kits

HumanHT-12 v3 Expression BeadChip Kits

The HumanHT-12 v3 Expression BeadChip content provides genome-wide transcriptional coverage of well-characterized genes, gene candidates, and splice variants. HumanHT-12 contains the same panel of probes as the HumanWG-6 BeadChip, but provides higher throughput processing of 12 samples per BeadChip. The high-value content provides genome-wide association studies and expresion-based quantitative trait loci (dQTL) studies.

Additional Details

BD-103-0203
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HumanWG-6 v3.0 Expression BeadChip Kits

HumanWG-6 v3.0 Expression BeadChip Kits

The HumanWG-6 v3.0 Expression BeadChip contains six arrays on a single BeadChip, each with >48,000 probes derived from human genes in the NCBI RefSeq and UniGene databases. Each array on the BeadChip provides genome-wide transcriptional coverage of well-characterized genes, gene candidates, and splice variants.

Additional Details

BD-101-0203
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MouseRef-8 v2.0 Expression BeadChip Kits

MouseRef-8 v2.0 Expression BeadChip Kits

Illumina’s MouseRef-8 v2.0 Expression BeadChips offer the most up-to-date content for mouse whole-genome expression profiling. Featuring content derived from the NCBI RefSeq database, these BeadChips reflect latest advancements in mouse genomics and provide the most biologically relevant information for murine genome studies.

Additional Details

BD-202-0202
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MouseWG-6 v2.0 Expression BeadChip Kits

MouseWG-6 v2.0 Expression BeadChip Kits

Illumina’s MouseWG-6 v2.0 Expression BeadChips offer the most up-to-date content for mouse whole-genome expression profiling. Featuring content derived from the NCBI RefSeq database, these BeadChips reflect latest advancements in mouse genomics and provide the most biologically relevant information for murine genome studies.

Additional Details

BD-201-0202
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RatRef-12 Expression BeadChip Kits

RatRef-12 Expression BeadChip Kits

The RatRef-12 Expression BeadChip for genome-wide expression analysis contains 21,910 probes selected primarily from the NCBI RefSeq database (Release 16).

Additional Details

BD-27-303
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Whole-Genome DASL Assay Kits

Whole-Genome DASL Assay Kits

The Whole-Genome DASL Assay greatly increases the DASL Assay target set, while retaining the ability to accurately profile partially degraded RNA samples. The assay combines the unique PCR and labeling steps of the DASL Assay with the gene-based hybridization and whole-genome probe set of the Illumina HumanRef-8 BeadChip.

Additional Details

DA-903-0024
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GoldenGate Methylation Cancer Panel I

GoldenGate Methylation Cancer Panel I

The GoldenGate Methylation Cancer Panel I provides researchers with a method for performing genetic association studies. It spans 1,505 CpG loci selected from 807 genes that fall into various classes, including tumor suppressor genes, oncogenes, genes involved in DNA repair, cell cycle control, differentiation, apoptosis, X-linked, and imprinted genes.

Additional Details

GM-17-211
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HumanRef-8 Expression BeadChip

HumanRef-8 Expression BeadChip

The HumanRef-8 v3.0 Expression BeadChip features up-to-date content derived from the National Center for Biotechnology Information Reference Sequence (NCBI RefSeq) database (Build 36.2, Release 22). The BeadChip targets approximately 24,500 well-annotated RefSeq transcripts and enables the interrogation of eight samples in parallel.

Additional Details

BD-102-0203
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HumanHT-12 v4 Expression BeadChip Kits

HumanHT-12 v4 Expression BeadChip Kits

The HumanHT-12 v4 Expression BeadChip content provides genome-wide transcriptional coverage of well-characterized genes, gene candidates, and splice variants. HumanHT-12 delivers high throughput processing of 12 samples per BeadChip without the need for expensive, specialized automation. The BeadChip is designed to support flexible usage across a wide-spectrum of experiments.

Additional Details

BD-103-0204
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Bovine SNP50 DNA Analysis Kits

Bovine SNP50 DNA Analysis Kits

The Bovine SNP50 DNA Analysis BeadChip contains 54,001 highly informative SNPs uniformly distributed across the entire genome of major cattle breed types. This empowers applications such as genome-wide enabled selection, identification of quantitative trait loci, evaluation of genetic merit of individuals, and comparative genetic studies.

Additional Details

WG-31-120
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Infinium Multi-Use Sample Preparation Kits

Infinium Multi-Use Sample Preparation Kits

The 2010 GWAS product roadmap for the Omni family of microarrays provides researchers with favorable pricing and the fastest access to new variants discovered by the 1000 Genomes Project. Researchers on the roadmap can begin genome-wide association studies immediately and add new variants through supplemental arrays as they become available. With the Infinium Multi-Use Sample Preparation kits, DNA samples require only a single amplification. Sample aliquots can then be stored and reused once new variants are available, while continuing to produce high-data quality over each usage.

Additional Details

WG-311-1123-PRE
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450K Infinium Methylation BeadChip Kits

450K Infinium Methylation BeadChip Kits

The 450K Infinium Methylation BeadChip's unique combination of comprehensive, expert-selected coverage, high sample throughput, and affordable price will make it an ideal solution for large sample-size genome-wide DNA methylation studies, such as the screening of genome-wide association study (GWAS) populations.

Additional Details

WG-314-1001-PRE
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HumanOmni2.5-Quad BeadChip Kits

HumanOmni2.5-Quad BeadChip Kits

The HumanOmni2.5-Quad (Omni2.5) BeadChip offers the most optimal and comprehensive set of both common and rare SNP content from the 1kGP (MAF>2.5%) for diverse world populations. Using the proven iScan or HiScanSQ System, this 4-sample BeadChip offers not only high throughput, but optimized tag SNP content from recently released 1000 Genomes Project pilot data. With the highest data quality and cutting edge content, including full support of copy number variation (CNV) applications, this powerful genotyping tool allows you to make more meaningful discoveries and publish faster.

Additional Details

WG-311-2504-PRE
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Human660W-Quad v1 DNA Analysis BeadChip Kits

Human660W-Quad v1 DNA Analysis BeadChip Kits

The Human660W-Quad BeadChip, built on the HumanHap550 BeadChip, offers comprehensive genomic coverage across many populations and the majority of known variation in regions of the genome, based on HapMap release 24 data. The entire panel of nearly 660,000 markers provides exceptional identification of known and novel structural variants.

Additional Details

WG-311-1501
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HumanOmniExpress BeadChip Kits

HumanOmniExpress BeadChip Kits

The HumanOmniExpress (OmniExpress) BeadChip delivers superior power for genome-wide association studies (GWAS), providing high sample throughput and comprehensive genomic content at the industry’s best price.

Additional Details

WG-311-1120-PRE
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HumanOmni1-Quad BeadChip Kits

HumanOmni1-Quad BeadChip Kits

The completely redesigned four-sample HumanOmni1-Quad BeadChip contains aggressively selected SNPs and probes that capture more genomic variation and provide the best power for GWAS and CNV discovery. Cutting-edge content includes markers derived from the 1,000 Genomes Project, all three HapMap phases, and recently published studies.

Additional Details

WG-311-1110
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BovineHD DNA Analysis Kits

BovineHD DNA Analysis Kits

Developed through a collaboration between Illumina scientists and leading bovine thought leaders, the BovineHD BeadChip features more than 777,000 evenly spaced SNPs that provide comprehensive coverage of the bovine genome, enabling a diverse range of genetic research applications. This eight-sample BeadChip, along with the proven Infinium HD Assay, presents a powerful high-throughput solution for whole-genome studies in any breed of beef and dairy cattle.

Additional Details

WG-450-1002
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cBot Single Read Cluster Generation Kit

cBot Single Read Cluster Generation Kit

The cBot Single Read Cluster Generation Kit provides reagents that bind DNA library samples to complementary adapter oligonucleotides grafted on the flow cell surface. The pre-mixed, 96-well plate format reagents in this kit provide a streamlined workflow with no reagent preparation and a total of 10 minutes hands-on time.

Additional Details

GD-300-1001
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cBot Paired-End Cluster Generation Kit

cBot Paired-End Cluster Generation Kit

The cBot Paired-End Cluster Generation Kit provides reagents that bind samples to complementary adapter oligos on the flow cell. These enable copying of the DNA strand after the first sequencing run; the copied strand is used to sequence the other fragment end. The cBot amplifies attached DNA fragments to clonal clusters of ~1000 copies each.

Additional Details

PE-300-1001
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HiSeq 2000 Paired-End Cluster Generation Kit

HiSeq 2000 Paired-End Cluster Generation Kit

The HiSeq Paired-End Cluster Generation Kit provides reagents that bind samples to complementary adapter oligos on the flow cell. These enable copying of the DNA strand after the first sequencing run; the copied strand is used to sequence the other fragment end. cBot amplifies attached DNA fragments to clonal clusters of ~1000 copies each.

Additional Details

PE-401-1001
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HiSeq 2000 Single-Read Cluster Generation Kit

HiSeq 2000 Single-Read Cluster Generation Kit

The HiSeq Single-Read Cluster Generation Kit provides reagents that bind samples to complementary adapter oligos on the flow cell.

Additional Details

GD-401-1001
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Small RNA Sample Prep Kit

Small RNA Sample Prep Kit

With Small RNA Discovery and Analysis, Illumina scientists have designed a sample preparation protocol that enables sequencing of of known and novel microRNAs as well as other non-coding RNAs, such as piwi-interacting RNAs and siRNAs. Sequencing-based Small RNA Sample Prep Kits offer researchers the flexibility to select the length of the small RNA they wish to investigate, enabling size-focused or broad size range investigation of different classes of small RNA on one universal platform.

Additional Details

FC-102-1009
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Paired-End DNA Sample Prep Kit V1

Paired-End DNA Sample Prep Kit V1

The Paired-End DNA Sample Prep Kit helps build DNA libraries for paired-end sequencing with insert sizes from 200-500 bp. Preparation includes introduction of two unique sequencing primer binding sites and adapter sequences to the anti-parallel strands of the polished whole-genome DNA fragments followed by gel-based size selection and purification.

Additional Details

PE-102-1001
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mRNA-Seq 8-Sample Prep Kit

mRNA-Seq 8-Sample Prep Kit

The mRNA-Seq 8-Sample Prep Kit is used to build DNA libraries for single-read and paired-end sequencing on the Genome Analyzer. Sample preparation is straightforward, using standard molecular biology techniques and requiring minimal hands-on time. mRNA template libraries are sequenced just as any DNA sample using Illumina Sequencing.

Additional Details

RS-100-0801
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Multiplexing Sample Preparation Oligonucleotide Kit

Multiplexing Sample Preparation Oligonucleotide Kit

The Multiplexing Sample Preparation Oligonucleotide Kit contains 12 unique oligonucleotides to “tag” libraries for pooling in one flow cell lane. Up to 96 samples can be sequenced on a single flow cell using the Genome Analyzer. The multiplex sequencing process is fully automated using the Cluster Station, Genome Analyzer, and Paired-End Module.

Additional Details

PE-400-1001
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Mate Pair Library Prep Kit

Mate Pair Library Prep Kit

The Mate Pair Library Prep Kit includes reagents needed to generate libraries with inserts from 2-5 kb in size. Prepared libraries consist of short fragments made up of two segments that were originally separated by several kilobases in the genome. Mate Pairs are sequenced using a two-adapter strategy identical to the paired-end sequencing method.

Additional Details

PE-112-1002
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Genomic DNA Sample Prep Kits

Genomic DNA Sample Prep Kits

Go from purified genomic DNA to a DNA library. Genomic DNA Sample Prep Kits include reagents to build DNA libraries for single-read sequencing. Random size–selected fragments of DNA are created, polished, and prepared for the addition of unique adapters to fragment ends. Following a short PCR enrichment, the library is ready to load.

Additional Details

FC-102-1001
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Tag Profiling Sample Prep Kits

Tag Profiling Sample Prep Kits

Tag Profiling Sample Prep Kits are used to build constructs comprised of a unique, positionally known 20- or 21-base pair cDNA tag with defined adapters attached to both ends. Access to any mRNA is through two restriction enzyme tag construction options. Kits are available complete or containing only the required oligonucleotides.

Additional Details

FC-102-1005
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ChIP-Seq DNA Sample Prep Kit

ChIP-Seq DNA Sample Prep Kit

Chromatin immunoprecipitation (ChIP) selectively finds DNA sequences bound by a particular protein. The ChIP-Seq DNA Sample Prep Kit helps build DNA libraries. The ChIP process enriches specific crosslinked DNA protein complexes using an antibody and unique oligonucleotide adapters added to small stretches of DNA bound to the protein of interest.

Additional Details

IP-102-1001
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Multiplexing Sequencing Primers and PhiX Control Kit V2

Multiplexing Sequencing Primers and PhiX Control Kit V2

The Multiplexing Sequencing Primers and PhiX Control Kit V2 is used to sequence samples tagged by using the Multiplexing Sample Preparation Oligonucleotide Kit and then amplified in the cBot or Cluster Station. Sequencing is fully automated on an Illumina sequencing system.

Additional Details

PE-400-2002
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HumanOmni1S-8 BeadChip Kits

HumanOmni1S-8 BeadChip Kits

The HumanOmni1S-8 (Omni1S) BeadChip is a remarkably priced tool for rapid integration of new rare 1000 Genomes content onto the Omni1/Express for 2-2.5M total variants (targeting MAF> 2.5%). Using the proven iScan or HiScanSQ System, this 8-sample BeadChip offers not only high throughput, but optimized tag SNP content from recently released 1000 Genomes Project pilot data. With the highest data quality and cutting edge content, including full support of copy number variation (CNV) applications, this powerful genotyping tool allows you to make more meaningful discoveries and publish faster.

Additional Details

WG-311-1114-PRE
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TruSeq SBS V5 HS kits

TruSeq SBS V5 HS kits

TruSeq SBS V5 HS kits contain ready-to-load reagents for accurately determining the DNA sequence of each cluster on a flow cell using sequencing by synthesis technology on the HiSeq 2000 sequencing system.

Additional Details

FC-401-1001
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Bovine3k Genotyping Kits

Bovine3k Genotyping Kits

Developed through a collaboration between Illumina and USDA-ARS, the Bovine3K BeadChip features 2,900 strategically selected SNPs that span the bovine genome, providing a high capacity to predict genetic merit for a number of important traits. This 32-sample BeadChip, along with the proven GoldenGate Assay, presents a cost-effective, high-throughput solution for accurate genetic analysis in many breeds of beef and dairy cattle.

Additional Details

GT-450-1001
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