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INNOgens

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Columbia, South Carolina, US

About INNOgens

INNOVATIVE GENOMICS SOLUTIONS (INNOgens) located in Columbia, South Carolina, offers high-quality DNA/RNA extraction, gene-microarrays on multiple platforms, Next Generation Sequencing (NGS), real-time quantitative PCR (RQ-PCR) and other molecular biology services for both clinical and research needs on... Show more »

INNOVATIVE GENOMICS SOLUTIONS (INNOgens) located in Columbia, South Carolina, offers high-quality DNA/RNA extraction, gene-microarrays on multiple platforms, Next Generation Sequencing (NGS), real-time quantitative PCR (RQ-PCR) and other molecular biology services for both clinical and research needs on bio-specimens, including fresh tissue, blood and fluid specimens, and FFPE.

Our management team brings together unique and innovative qualities in clinical and research serveices. Our team combines unparalleled scientific and medical knowledge as well as the operational expertise developed through decades of working in research, pharma, clinical and CRO industrial. Our laboratory team includes all PhD/MD scientists, each with over 10 years of experience in Molecular Biology, Genetics and Next Gen Sequencing. We provide services at a low price and the quality of our results cannot be matched. All services are performed in the USA to ensure a quick turnaround time, readily available technical support, and unprecendented reliability.

INNOgens follows strict workflow guidelines set by the American College of Medical Genetics (ACMG) and Clinical Laboratory Improvement Amendments (CLIA) by the Center for Medicare & Medicaid Services (CMS) and South Carolina Department of Health & Environmental Control (DHEC).

INNOgens is licensed as a Clinical Laboratory by the South Carolina Department of Health & Environmental Control (DHEC) for the purpose of performing genetic testing and sequencing. INNOgens is approved to accept human specimens.

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Our Services (33)


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Next Generation Sequencing (NGS)

Price on request
Request a quote for more information about this service.

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DNA/RNA Analysis and Quality Control

Price on request
Request a quote for more information about this service.
Agilent Bioanalyzer

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DNA Extraction

Price on request

We provide customized nucleotide extraction solutions. The quality of the STARTING MATERIAL (DNA or RNA) is one of the most important factors for genomics downstream application. We offer customers a large number of qualified, AUTOMATED or MANUAL methods using popular reagent kits to support your research needs. View our current... Show more »

We provide customized nucleotide extraction solutions. The quality of the STARTING MATERIAL (DNA or RNA) is one of the most important factors for genomics downstream application. We offer customers a large number of qualified, AUTOMATED or MANUAL methods using popular reagent kits to support your research needs. View our current SERVICES list below:
Types of DNA Extraction Services:
☐ Human and animal samples:
• Blood and blood products including blood cards, serum/plasma;
• Saliva;
• Swabs;
• Tissues: FFPE sections/cores, Fresh frozen tissue, cultured cells
☐ Plant samples: fresh/frozen/lyophilized leaves, seeds
☐ Microbial samples: bacteria, yeasts, filamentous fungi, viruses
☐ Food and environmental samples: processed foods, soil, water, sewer sludge
☐ Forensic samples: dry blood spots, buccal swab, FTA cards, semen spots, hairs, cigarette butts
Let us know if your sample is not listed or you have specific requirements, our technical support team will work with you to find right solution.

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KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5

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qPCR

Quantitative PCR
Price on request

Real-Time PCR (RT-PCR), or Realtime quantitative PCR (RQ-PCR), is a quantitation method extensively used for DNA copy number detection, gene expression, SNP genotyping, adventitious agent detection, and many other applications in the fields of genomics research, drug R&D, biologics testings and clinical diagnostics and threaputic... Show more »

Real-Time PCR (RT-PCR), or Realtime quantitative PCR (RQ-PCR), is a quantitation method extensively used for DNA copy number detection, gene expression, SNP genotyping, adventitious agent detection, and many other applications in the fields of genomics research, drug R&D, biologics testings and clinical diagnostics and threaputic monitoring. Leveraged with extensive experience in RQ-PCR assay design, validation, and testing, and equipped with an ABI 7900 HT Sequence Detection System, INNOgens offers a variety of real-time PCR services to clients.

In clinical application of routine diagnosis of diseases, particularly for cancer and infection diseases, this molecular tool is well-suited for the rapid detection directly in clinical specimens, allowing early, sensitive and specific laboratory confirmation of related diseases. This method also allows a rapid assessment of the presence of resistance genes or gene mutations. Although this genetic approach is not always predictive of phenotypic resistances, in specific situations it may help to optimize the therapeutic management of patients.

It also is suitable for the diagnosis of infections caused by fastidious growth species, and the number of these pathogens has increased recently.

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KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5

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Small RNA Sequencing

Price on request

small RNAs (smRNA) are short, non-coding RNA molecules that can regulate gene expression in both the cytoplasm and the nucleus via post-transcriptional gene silencing (PTGS), chromatin-dependent gene silencing (CDGS) or RNA activation (RNAa). miRNAs play an important role in many biological processes, including differentiation and... Show more »

small RNAs (smRNA) are short, non-coding RNA molecules that can regulate gene expression in both the cytoplasm and the nucleus via post-transcriptional gene silencing (PTGS), chromatin-dependent gene silencing (CDGS) or RNA activation (RNAa). miRNAs play an important role in many biological processes, including differentiation and development, cell signaling, and response to infection. In recent years microRNAs (miRNAs) have been established as important biomarkers in a variety of diseases including cancers, diabetes, cardiovascular diseases, aging, Alzheimer's disease, etc.

Circulating miRNAs are detectable in serum and plasma, and the level of their expression varies as a result of disease which presents great potential for circulating miRNA expression signatures to be used as biomarkers in disease diagnosis and prevention.

NGS smRNA sequencing, a new method and a powerful tool to identify and quantitatively decode the entire population of smRNAs, is now available in addition to existing microarray and qRT-PCR profiling services. We offer a one-stop solution for your smRNA including miRNA discovery and expression profiling.

Understanding miRNA sequencing and smRNA sequencing

  • miRNA sequencing is dependent on gel extraction of a band representing an insert size of 18-30+ nucleotides in length; this assures that contamination of degraded RNA, empty adaptors or primer dimers is minimal in the NGS microRNA library.
  • smRNA sequencing is dependent on excision of a custom size for library construction (in the 30-200 nucleotide range), which can include microRNAs, pre-microRNAs, tRNAs, snRNAs, snoRNAs, piRNAs and other small RNA molecules in this size range.
  • miRNA and smRNAs have to be separately sequenced in the same sample as it is not possible to compare expressions levels of RNA species with different length with any confidence.
  • smRNA sequencing can only be performed on high quality RNA. Partially degraded RNA or RNA from FFPE samples contains large quantities of degraded rRNAs and mRNA resulting in a large portion of the sequencing reads being irrelevant. It requires to sequence with a greater number of reads to capture sufficient relevant reads.

Consultation and experimental design for your project

Please contact INNOgens to discuss your project and arrange a free consultation with our NGS experts. Our scientists will discuss with you in detail to help you design your experiment.

  • When you engage INNOgens service for your smRNA/miRNA NGS projects, you are assured direct communication with the scientists performing your experiments throughout the duration of the project.
  • Each project begins with a free consultation with a smRNA/miRNA NGS expert. We design an experimental setup that best satisfies your project needs and budget, and customers can be ensured that all experimental details and subsequent analysis are clearly defined and understood by both parties.

Our Comprehensive Service

  • We offer two small RNA sequencing services; 1) miRNA sequencing and 2) smRNA sequencing. miRNA sequencing is specifically focused on discovery and quantification of miRNAs. This includes novel miRNA detection and prediction. smRNA sequencing is specifically for other smRNA targets such as sn/sno/tRNA/piRNA.Using NGS high-throughput sequencing technology, our smRNA discovery service enables sequencing and profiling of all types of smRNAs with high sensitivity.
  • Our “Sample to Data” comprehensive service includes: sample preparation (small RNA selection, library preparation, and library amplification), sample QC at important steps, high-throughput sequencing, bioinformatics analysis, and a customer data report.
  • Down-stream profiling of identified (and other customer defined target miRNAs) is also available by custom microarray and qPCR analysis services.

Service Details:

  • SmRNA/miRNA isolation service from cells, tissues, liquid biopsy (Plasma/Serum)
  • cDNA synthesis of smRNA and miRNA
  • smRNA/miRNA library preparation of cDNA
  • Production of cDNA from RNA for smRNA profiling (NGS)
  • miRNA profiling service (miRNA microarray)
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RNA Sequencing

Price on request

RNA-Seq is a technology that uses Next Generation Sequencing to perform transcriptome profiling. Studies using this method have already changed our view of the extent and complexity of eukaryotic transcriptomes because it provides a far more precise measurement of levels of transcripts and their isoforms than other methods. RNA... Show more »

RNA-Seq is a technology that uses Next Generation Sequencing to perform transcriptome profiling. Studies using this method have already changed our view of the extent and complexity of eukaryotic transcriptomes because it provides a far more precise measurement of levels of transcripts and their isoforms than other methods. RNA Seq supports multiple applications including:

  • Transcriptome analysis (complete set of all transcripts in a cell) - Detection of all transcripts present in a sample, with the ability to detect rare transcripts by increasing sequencing depth.
  • Splice variant analysis - The relative expression of exons across a single transcript can elucidate the presence of splice variants.
  • Differential expression analysis- The differential expression levels of two transcripts in a single sample or of transcripts in two disparate samples can be ascertained from relative sequencing depths.
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KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5

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Whole Exome Sequencing (WES)

Price on request

Exome sequencing is a technique for sequencing all the protein-coding genes (known as the exome) utilizing probes to capture exome regions selectively from an entire genome. Using this technology, exome sequencing allows for the identification of gene mutations associated with common diseases.

INNOgens now provides whole... Show more »

Exome sequencing is a technique for sequencing all the protein-coding genes (known as the exome) utilizing probes to capture exome regions selectively from an entire genome. Using this technology, exome sequencing allows for the identification of gene mutations associated with common diseases.

INNOgens now provides whole exome sequencing services, which combines sample QC, DNA fragmentation and library preparation, target enrichment, Illumina sequencing, and data analysis. Your project will be fully supported by a team of scientists and bioinformaticians to provide the highest quality results.

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KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5

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Illumina NGS Library Preparation

Price on request

A next generation sequencing (NGS) library is built up of random DNA fragments that represent the entire genetic information in the sample. Preparation of high quality libraries with high yield is a critical first step in the NGS process, and library preparation can be made using series of standard molecular biology reactions. It... Show more »

A next generation sequencing (NGS) library is built up of random DNA fragments that represent the entire genetic information in the sample. Preparation of high quality libraries with high yield is a critical first step in the NGS process, and library preparation can be made using series of standard molecular biology reactions. It is created by shearing DNA into fragments of varying sizes (180 - 400 bp). These fragments are ligated to specific adapters. Library fragments of the appropriate size are then selected and isolated. Following a sample cleanup step, the resultant library is quantified by qPCR and checked for quality using the Agilent Bioanalyzer.

RNA or DNA is extracted from sample tissue/cells and fragmented. RNA is converted to cDNA by reverse transcription. DNA Fragments are converted into the library by ligation to sequencing adapters containing specific sequences designed to interact with the NGS platform, either the surface of the flow-cell (Illumina) or beads (Ion Torrent). The next step involves clonal amplification of the library, by either cluster generation for Illumina or microemulsion PCR for Ion Torrent. The final step generates the actual sequence via the chemistries for each technology.

We provide high quality services that facilitate library preparation of DNA, total RNA/mRNA and small RNA for downstream applications such as next generation sequencing and expression library construction. With a collection of NGS library preparation methods using commercially available products/kits INNOgens has established a standard protocol for library preparation for most applications, and provides for library preparation for Illumina, and Ion Torrent sequencing platforms, and is available in multiple formats, including reagents sets, master mix sets and modules for whole exome, RNA Seq (from total RNA, RNA low-level detection, rRNA/hemoglobin mRNA depleted RNA, and small RNA), and targeted panel library preparations.

Starting Materials

  • Starting materials can include fragmented dsDNA isolated from various tissue or cell samples, dsDNA enriched from ChIP reactions, MeDIP/hMeDIP reactions, or exon capture.
  • DNA should be relatively free of RNA since large fractions of RNA will impair end repair and dA tailing, resulting in reduced ligation capabilities.
  • Input amount of DNA can be from a few ng to about 2 µg. For amplification-free applications, more starting material is required.
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Agilent DNA Microarray

Price on request

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in... Show more »

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in INNOgen's state-of-the-art genomics laboratory. Whether you outsource your entire genetic research needs or just your backlog samples, our high-throughput capacity ensures rapid delivery of high-quality results.

Our instrumentation includes a complete Affymetrix GeneChip System and Agilent′s SureScan High Resolution Scanner and related equipment. We are equipped with all necessary ancillary equipment including a NanoDrop 2000c Spectrophotometer, an Agilent 2100 Bioanalyzer, refrigerated centrifuges, an ABI 3730 DNA Analyzer, an ABI PRISM® 7900HT Sequence Detection System, and a Savant DNA 110 Speed Vac.

Our microarray lab processes RNA and DNA for hybridization to all available arrays through either Agilent or Affymetrix , and addresses diverse research needs from a few samples to hundreds, and targeted to genome-wide analysis. The amount of required input RNA/DNA needed varies from about 50 ng to a few ug depending on the array type. Each RNA/DNA sample we receive will be evaluated for its quality and quantity, amplified, fragmented, and fluorescently labeled before being hybridized to an array following our standardized protocol. Bound nucleic acids will be visualized by fluorescent dye detection with our high resolution scanner. All the procedures from start to finish, including sample QC, labeling and hybridization take three-four days. The data files will be provided to end users for bioinformatics analysis.

Highlights:

  • Immediate and cost effective access to high resolution aCGH chromosome and SNPs analysis; and precise/reliable gene expression
  • The capacity to fulfill your entire current and future genomic research requirements.
  • Fast, reproducible and consistent high quality results. Our genomic services laboratory specializes in handling, tracking and processing large numbers of samples delivering high quality data with tight deadlines.
  • Peace-of-mind through complete sample tracking and expertise at every step of the process. We have excellent experience in project management (including reagents, consumables and equipment maintenance) and are able to monitor every step in the microarray workflow. We have established a set of QC metrics which enables you to have complete confidence in the quality, reproducibility and speed of our service.
  • An industry-leading microarray analysis package with full technical support.
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KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5 Agilent

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Agilent RNA Microarray

Price on request

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in... Show more »

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in INNOgen's state-of-the-art genomics laboratory. Whether you outsource your entire genetic research needs or just your backlog samples, our high-throughput capacity ensures rapid delivery of high-quality results.

Our instrumentation includes a complete Affymetrix GeneChip System and Agilent′s SureScan High Resolution Scanner and related equipment. We are equipped with all necessary ancillary equipment including a NanoDrop 2000c Spectrophotometer, an Agilent 2100 Bioanalyzer, refrigerated centrifuges, an ABI 3730 DNA Analyzer, an ABI PRISM® 7900HT Sequence Detection System, and a Savant DNA 110 Speed Vac.

Our microarray lab processes RNA and DNA for hybridization to all available arrays through either Agilent or Affymetrix , and addresses diverse research needs from a few samples to hundreds, and targeted to genome-wide analysis. The amount of required input RNA/DNA needed varies from about 50 ng to a few ug depending on the array type. Each RNA/DNA sample we receive will be evaluated for its quality and quantity, amplified, fragmented, and fluorescently labeled before being hybridized to an array following our standardized protocol. Bound nucleic acids will be visualized by fluorescent dye detection with our high resolution scanner. All the procedures from start to finish, including sample QC, labeling and hybridization take three-four days. The data files will be provided to end users for bioinformatics analysis.

Highlights:

  • Immediate and cost effective access to high resolution aCGH chromosome and SNPs analysis; and precise/reliable gene expression
  • The capacity to fulfill your entire current and future genomic research requirements.
  • Fast, reproducible and consistent high quality results. Our genomic services laboratory specializes in handling, tracking and processing large numbers of samples delivering high quality data with tight deadlines.
  • Peace-of-mind through complete sample tracking and expertise at every step of the process. We have excellent experience in project management (including reagents, consumables and equipment maintenance) and are able to monitor every step in the microarray workflow. We have established a set of QC metrics which enables you to have complete confidence in the quality, reproducibility and speed of our service.
  • An industry-leading microarray analysis package with full technical support.
Show less
KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5 Agilent

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Affymetrix RNA Microarray

Price on request

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in... Show more »

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in INNOgen's state-of-the-art genomics laboratory. Whether you outsource your entire genetic research needs or just your backlog samples, our high-throughput capacity ensures rapid delivery of high-quality results.

Our instrumentation includes a complete Affymetrix GeneChip System and Agilent′s SureScan High Resolution Scanner and related equipment. We are equipped with all necessary ancillary equipment including a NanoDrop 2000c Spectrophotometer, an Agilent 2100 Bioanalyzer, refrigerated centrifuges, an ABI 3730 DNA Analyzer, an ABI PRISM® 7900HT Sequence Detection System, and a Savant DNA 110 Speed Vac.

Our microarray lab processes RNA and DNA for hybridization to all available arrays through either Agilent or Affymetrix , and addresses diverse research needs from a few samples to hundreds, and targeted to genome-wide analysis. The amount of required input RNA/DNA needed varies from about 50 ng to a few ug depending on the array type. Each RNA/DNA sample we receive will be evaluated for its quality and quantity, amplified, fragmented, and fluorescently labeled before being hybridized to an array following our standardized protocol. Bound nucleic acids will be visualized by fluorescent dye detection with our high resolution scanner. All the procedures from start to finish, including sample QC, labeling and hybridization take three-four days. The data files will be provided to end users for bioinformatics analysis.

Highlights:

  • Immediate and cost effective access to high resolution aCGH chromosome and SNPs analysis; and precise/reliable gene expression
  • The capacity to fulfill your entire current and future genomic research requirements.
  • Fast, reproducible and consistent high quality results. Our genomic services laboratory specializes in handling, tracking and processing large numbers of samples delivering high quality data with tight deadlines.
  • Peace-of-mind through complete sample tracking and expertise at every step of the process. We have excellent experience in project management (including reagents, consumables and equipment maintenance) and are able to monitor every step in the microarray workflow. We have established a set of QC metrics which enables you to have complete confidence in the quality, reproducibility and speed of our service.
  • An industry-leading microarray analysis package with full technical support.
Show less
KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5 Affymetrix

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Affymetrix Microarray

Price on request

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in... Show more »

INNOgens provides comprehensive Microarray Analysis Services featuring the Affymetrix and Agilent microarray platforms. The content for these arrays has been carefully selected to enable reliable and reproducible identification of changes in gene expression, SNPs, and epigenetic alterations. The arrays will be processed in INNOgen's state-of-the-art genomics laboratory. Whether you outsource your entire genetic research needs or just your backlog samples, our high-throughput capacity ensures rapid delivery of high-quality results.

Our instrumentation includes a complete Affymetrix GeneChip System and Agilent′s SureScan High Resolution Scanner and related equipment. We are equipped with all necessary ancillary equipment including a NanoDrop 2000c Spectrophotometer, an Agilent 2100 Bioanalyzer, refrigerated centrifuges, an ABI 3730 DNA Analyzer, an ABI PRISM® 7900HT Sequence Detection System, and a Savant DNA 110 Speed Vac.

Our microarray lab processes RNA and DNA for hybridization to all available arrays through either Agilent or Affymetrix , and addresses diverse research needs from a few samples to hundreds, and targeted to genome-wide analysis. The amount of required input RNA/DNA needed varies from about 50 ng to a few ug depending on the array type. Each RNA/DNA sample we receive will be evaluated for its quality and quantity, amplified, fragmented, and fluorescently labeled before being hybridized to an array following our standardized protocol. Bound nucleic acids will be visualized by fluorescent dye detection with our high resolution scanner. All the procedures from start to finish, including sample QC, labeling and hybridization take three-four days. The data files will be provided to end users for bioinformatics analysis.

Highlights:

  • Immediate and cost effective access to high resolution aCGH chromosome and SNPs analysis; and precise/reliable gene expression
  • The capacity to fulfill your entire current and future genomic research requirements.
  • Fast, reproducible and consistent high quality results. Our genomic services laboratory specializes in handling, tracking and processing large numbers of samples delivering high quality data with tight deadlines.
  • Peace-of-mind through complete sample tracking and expertise at every step of the process. We have excellent experience in project management (including reagents, consumables and equipment maintenance) and are able to monitor every step in the microarray workflow. We have established a set of QC metrics which enables you to have complete confidence in the quality, reproducibility and speed of our service.
  • An industry-leading microarray analysis package with full technical support.
Show less
KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5 Affymetrix

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Comprehensive Cancer Gene Panel

Price on request

INNOgens is offering the truly end-to-end Next Generation Sequencing (NGS) workflow solution for various cancers from primary fresh frozen or FFPE sample to a final report that provides a simpler, more cost-effective way for clinical testing.

Multiple Cancer-Related Gene Panels and Its Specifications

Our targeted panels... Show more »

INNOgens is offering the truly end-to-end Next Generation Sequencing (NGS) workflow solution for various cancers from primary fresh frozen or FFPE sample to a final report that provides a simpler, more cost-effective way for clinical testing.

Multiple Cancer-Related Gene Panels and Its Specifications

Our targeted panels are the simplest tools for analyzing the genetic variants of a focused panel of genes via NGS. Each panel consists of multiplex PCR primer sets to amplify exonic regions of a thoroughly researched panel of biologically and clinically relevant and disease-focused genes. The targeted disease panels can also be customized to include genes or other genomic regions tailored to your specific NGS project needs. Our high-quality primer design and targeted enrichment chemistry provide high design coverage, specificity, and uniformity, which are essential for detecting low-frequency variants in your precious samples.

Clinically and biologically relevant content

The Targeted Panels focus on specific mutations, exons, and genes that are most relevant to a particular cancer types. The content of these panels was selected from the College of American Pathologists (CAP) guidelines, NCCN guidelines, late-stage clinical trials, The Cancer Genome Atlas (TCGA), and Ingenuity® Knowledge Base.

Largest available collection of panels

More than 12 cataloged panels address distinct clinical and research analysis needs, ranging from precise detection of actionable mutations in solid tumors and hematologic malignancies to mutation profiling for specific cancer types.
Multiple Cancer-Related Gene Panels and Its Specifications.
Cancer-Related Gene Panels examine complex genetic information and provide extremely detailed and patient-oriented data, regarding the drivers of major cancers. Panels have the potential to uncover advanced genetic diagnoses, and provide prevention strategies and personalized treatments.

  • Accurate genetic mutation information for diagnoses and treatment through Next Generation Sequencing under CLIA regulation.
  • Analyses based on American College of Medical Genetics and Genomics (ACMG)-recommended genes, to offer patients more credible data.
  • Coverage of the most major cancers (Breast Cancer, Colon Cancer, Ovarian Cancer, Prostate Cancer, Gastric Cancer, Lung Cancer and other type of Cancer).

Testing Procedures

The targeted disease NGS is performed by Innovative Genomics Solutions. The individual’s genomic DNA is prepared from various tissues including fresh frozen and Formalin-fixed, paraffin-embedded (FFPE) tissues, whole blood; blood products, buccal swab. Sequencing analysis will be performed using various NGS platforms. Sequence variants are identified.

Reporting Results

The applications of cancer-related panels have the potential for enhancing personalized patient care. The applications include:

  • Identifying rare genetic mutations and variations including InDels.
  • Deeper analysis of targeted DNA regions.
  • Discovery of cancer-causing genetic mutations, and many more others. Each report includes a detailed explanation of all clinically-relevant variants.
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RNA Extraction and Purification

Price on request

Our RNA extraction methods are suitable for all types of RNA extraction including total RNA, mRNA and small RNA from various type of samples including FFPE and liquid biopsy. We utilize standardized commercially available kits that meet your project needs. Our goal is to find the best solutions for the customer and provide the... Show more »

Our RNA extraction methods are suitable for all types of RNA extraction including total RNA, mRNA and small RNA from various type of samples including FFPE and liquid biopsy. We utilize standardized commercially available kits that meet your project needs. Our goal is to find the best solutions for the customer and provide the highest quality RNA.

Following sample types are included:

  • Tissue: both fresh frozen and FFPE
  • Cells
  • Blood and blood products (Plasma/Serum)
  • Viruses
  • Plants
  • Bacteria
  • Others

RNA extracted by INNOgens is suitable for most downstream molecular biology applications:

  • Gene expression microarray
  • RNA sequencing and smRNA/miRNA sequencing
  • Real-time qPCR
  • Northern blot analysis
  • Transcriptome analysis
  • RNA cloning
  • RNA structure/function
  • Ribosomal RNA depletion
  • Others
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AmpliSeq NGS Panels

Price on request

AmpliSeq
AmpliSeq is a Multiplex PCR-based assay capable of targeting many different regions of genes. AmpliSeq provides fixed panels designed by leading professionals throughout various fields of study. Using AmpliSeq technology we can designate targets for custom panels and sequence just the needed information. You can create... Show more »

AmpliSeq
AmpliSeq is a Multiplex PCR-based assay capable of targeting many different regions of genes. AmpliSeq provides fixed panels designed by leading professionals throughout various fields of study. Using AmpliSeq technology we can designate targets for custom panels and sequence just the needed information. You can create your own panels or have our Project Manager/Scientists design a panel to your specifications.

Services / Applications
AmpliSeq Fixed Panels
Inherited Disease Panel
Comprehensive Cancer Panel
Cancer Hotspot Panel v2
BRCA1 and BRCA2 Panel
Colon, Breast, Lung, and liver Cancer Panels
Many others

AmpliSeq Custom Panels
Custom DNA AmpliSeq Panels
Design panels by sending us gene names, chromosomal coordinates, SNP rs# or uploading target lists.

Benefits of INNOgens' AmpliSeq NGS Services
Knowledgeable Technical Assistance
Fast Turnaround for Fixed Panels
Sequence with the depth of coverage that makes sense for your project
Multiplexing samples using validated indices lowers your costs
Library Construction
Multiple QC steps
High Quality Data
Variant Caller for SNP

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KingFisher FLEX Qiagen GeneReader Bio-Rad iQ5

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Clinical Molecular Diagnostics

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PCR

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DNA Library Preparation

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Biochemistry & Molecular Biology

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RNA Services

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Biology

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DNA Extraction and Purification

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Targeted Gene Sequencing

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Gene Panel Testing

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RNA Microarray

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DNA Microarrays

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Clinical Laboratory Services

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Clinical Research

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Exome Sequencing Services

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DNA Services

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Nucleic Acid Services

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DNA Sequencing

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RNA Microarray Platforms

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