Low Input, Degraded or FFPE Total RNA Sequencing
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Applied Biological Materials, Inc. is an Illumina Certified Service Provider, dedicated to ensuring the delivery of the highest-quality data available for genetic analysis applications. Click here for more details about the Illumina CSpro program.
  Offering new insights into genome organization and regulation.

Prices are in US dollars. Please contact technical@abmgood.com if you need a quotation in Canadian dollars.
Service/Description Cat. No. Min. Samples Price*
Single-End
Low Input / FFPE Total RNA Sequencing (8 million reads, 1x75bp SE) IR31008 2Inquire
Low Input / FFPE Total RNA Sequencing (20 million reads, 1x75bp SE) IR31020 2Inquire
Low Input / FFPE Total RNA Sequencing (40 million reads, 1x75bp SE) IR31040 2Inquire
Low Input / FFPE Total RNA Sequencing (80 million reads, 1x75bp SE) IR31080 2Inquire
 
Paired-End
Low Input / FFPE Total RNA Sequencing (8 million reads, 2x75bp PE) IR32008 2Inquire
Low Input / FFPE Total RNA Sequencing (20 million reads, 2x75bp PE) IR32020 2Inquire
Low Input / FFPE Total RNA Sequencing (40 Million Reads, 2x75bp PE) IR32040 2Inquire
Low Input / FFPE Total RNA Sequencing (80 Million Reads, 2x75bp PE) IR32080 2Inquire
 
Additional Sample Preparation Services
rRNA Depletion Treatment (human, mouse, or rat) IR16001 1$145.00*
rRNA Depletion Treatment (plant or bacteria) IR16002 1$145.00*
Total RNA Isolation for NGS IR19001 1$50.00*
 
Bioinformatics Analysis
Raw data provided in FASTQ format if none of the below services are selected.
Standard RNA-Seq Analysis
- Industry standard output in FASTQ format
- Read mapping & relative gene expression levels within a sample for HUMAN or MOUSE
- Reference Genome Import fee (see below) applies for other species
Included
Reference Genome Import
Free Reference Genome Import for Human or Mouse - Included
Reference Genome Import (<10Mb genome) IB00001 1$50.00^
Reference Genome Import (>10Mb genome) IB00002 1$200.00^
Comparisons Between Samples or Groups
Pairwise Comparison for mRNA IB00003 1$200.00**
Pariwise Comparison for miRNA IB00005 1$600.00**
Genome Assembly
Note: If there is an insufficient amount of reads to complete the assembly there will be a minimum charge of $350.
de novo Assembly & Transcript Identification IB00006 1$750.00*
Annotation (i.e. functional interpretation) IB00007 1$350.00*
de novo Assembly & Transcript Identification (Plant) IB00017 1$1500.00*
Sequencing Panel Analysis IB00018 1$35.00*
Genome Comparison
SNP Detection IB00008 1$350.00**
Novel Splice Junction Discovery IB00009 1$500.00**
Novel Isoform Discovery IB00010 1$500.00**
 
Quality Control Service
Sample and Library QC IR18001 1$50.00*
 
Data Storage Service
Data Storage (per additional 3 months) IS10001 1$150.00
*Price per Sample
^Price per Species
**Price per Comparison
Service Details
Description of Low Input, Degraded or FFPE RNA-Seq Service
    FFPE samples contain nucleic acids that historically have been too fragmented from the fixation protocol to derive meaningful data from, and in the case of RNA-Seq, nearly impossible to remove rRNA based fragments from. Since these tissues are an invaluable resource in clinical cancer research with regards to histological analysis, this has long presented a problem for next generation sequencing. However, abm’s new low input, degraded, or FFPE Total RNA Sequencing service uses a protocol specially designed for working with partially degraded FFPE samples or RNA samples with low RIN. This service uses Clontech’s SMARTer Universal Low Input RNA Kit designed for the purposes of sequencing rRNA-depleted total RNA from low input (10-100 ng/~1000-10,000 cells), degraded or FFPE samples. Like our standard RNA-Seq services, we can tailor our sequencing services to a wide spectrum of custom needs and provide minimal turnaround time.

Key features for abm's Low Input, Degraded or FFPE RNA-Seq Service:
  • Able to prepare NGS libraries from as little as 10ng (1000 cells) of total RNA.
  • Employs Clontech SMART technology (Switching Mechanism at 5’ End of RNA Template).
  • RNA strandedness is preserved.
  • Can use either polyA+ enriched or rRNA depleted total RNA as input.

Included in Low Input, Degraded or FFPE RNA-Seq Service:
  • Library Preparation and sequencing on the Illumina platform.
    • We accept rRNA-depleted Total RNA or polyA+ enriched RNA as input.
    • We can accept Total RNA, with rRNA depletion incurring an additional charge.
  • Read mapping (Tophat) and Gene expression quantification (Cufflinks/FPKM) for human or mouse (Reference Genome Import Fee may apply for other species).
  • QC (RSeQC/FastQC).
  • 3 months FREE storage of raw data.
Sample Requirement Guidelines Click To Open
Confidentiality of Low Input, Degraded or FFPE Total RNA Sequencing Results
    All customer information is held in strict confidence. All materials and information sent to us and the products produced by us for the order are the property of the customer and will be returned to the customer or discarded in a confidential manner. We only archive customer materials when instructed to.
Project Design/Advice
    Please email us at NGS@abmgood.com for assistance with starting your Low Input, Degraded or FFPE Total RNA Seq project or any inquiries about our next generation sequencing services. We offer discounts on bulk sample sequencing, please inquire for more details. ABM also provides an RNA purification service from original tissue samples for $50/sample. The minimum amount of RNA needed depends on the specific RNA preparation method pertinent for each project. A sample preparation guide for RNA Sequencing with ABM can be downloaded here.
Policies
    Our goal is always to deliver high-quality useful data to aid you in your research. We perform extensive maintenance and quality assurance on our equipment and strict quality control of samples throughout the sequencing process.However, next-generation sequencing by nature does not always deliver equally robust results due to a variety of factors, such as the variability inherent in the library preparation process, the biochemistry that takes place during sequencing and the quality of samples that we receive. We will make every effort to deliver the number of reads that are listed, although it is not possible to guarantee that those targets will always be achieved. The actual number of reads passing filter may vary by up to 10% from the listed target. Studies by various institutes have shown that there is minimal difference in coverage for 10% variation in reads past 5-10 million total reads.
Product Documents
Product References
FAQs
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Is your company certified as a service provider for Illumina sequencing?
Yes, we are a certified Illumina service provider.
What kind of analysis software do you use for sequence analysis?
The Illumina sequencers come with the integrated software that can perform the regular bioinformatics analysis functions. In addition, we have extensive experience with other open access software such as Galaxy, Adnuril, BioBike, etc. In other words, we are willing to perform additional bioinformatics analysis with different software and tools to satisfy a variety of demands from our customers.
What kind of QC methods do you adopt for the customer's sample(s)?
We will perform QC on your Total RNA samples prior to sequencing them, using the Agilent Bioanalyzer (industry standard) to determine the RNA Integrity Number (RIN). If the RIN is lower than 8, we consider these samples as having failed QC. If the samples do not pass QC, we will ask you to send us new samples. If we do not receive new samples, thereby cancelling the sequencing order, there will be a QC fee of $50/sample. This fee will be waived if you choose to continue with the sequencing order. A strict positive and negative control will be applied to this QC process.

The library QC will also be performed using the Agilent Bioanalyzer to determine library size and purity. Also, prior to loading the libraries on the sequencer, we perform qPCR quantification. The cost for this is included in the sequencing service.

For the QC of the final data from our sequencing service, the integrated software will generally do the job and provide adequate QC information, however, we can also provide additional QC data such as FASTQC upon request.

The data we output will pass our Q30 filter, which means that the error rate in base calls is less than 1 in 1000, or 0.1%. We will get a percentage at the end of the run which states the percentage of bases that have a Q score > 30, and this percentage is usually ≥85%.
What is the lead time for your WGS, WES, and RNA-Seq services?
Our sequencing lead times depend on workload, but are typically 2-4 weeks for sequencing data + 2-3 weeks for standard analysis. Please inquire for lead times for more detailed analysis.
Can you recommend any preferred RNA/DNA isolation kits to provide the best quality samples for these services?
For miRNA sequencing, you may isolate your RNA sample with a mirVana™ miRNA Isolation Kit,
mirVana™ PARIS™ Kit or PureLink® miRNA Isolation kit to enable adequate enrichment of your sample. If preferred, it should be okay to use Qiagen's kit, as long as the RNA Integrity Number (RIN) of the sample is above 8.0 to make sure there is no significant degradation. (Samples with a RIN lower than 8.0 may contain smaller degraded RNA fragments that can be sequenced in addition to the miRNAs). We prefer receiving Total RNA sample however so we can perform the bioanalyzer QC to check the RNA quality before beginning library construction. There will be no extra-charges if you submit Total RNA instead of isolated miRNA.

For miRNA sequencing we require 200ng-2ug of total RNA in 10ul of nuclease free water, as quantified with a fluorometric method. Lower amounts might result in inefficient ligation and low yield. If you are supplying purified miRNA, please submit a minimum of 50-100 ng of purified small RNA in 10ul is required. Purified small RNAs must be in nuclease free water or 10 mM Tris-HCI, pH 8.5.

For other services, there are generally no preferred DNA/RNA isolation kits as long as minimum requirements for QC are met.

Do I need any special software to view the data report files?
You will first need to unzip the fastq.gz files with winrar to view with vim, nano, gedit, Notepad plus plus. Nextgen workbench generally can view the data immediately without unzipping.

The RNASeq_sample_cufflinks_output.tar.gz will also need to be unzipped to see the text files by vim, nano, gedit, or Notepad plus plus. The unzipped data an also be imported as text into the data tab of Excel 2007. Other versions may differ.

To analyze further, Excel can sort, filter, find, match, etc and has many functions for conditional coloring, graphing, etc.
For the data, why are there no "ALT", "POS" and "ID" in your CSV file?
CSV files are meant to be used in conjunction with the raw fastq/bam files by certain commercial bioinformatics software. Many have a proprietary algorithms that takes the ALT POS and ID from the Fastq and indexes them for its own use. They are not meant to be used alone.
Would you let me know the description for the following: Genotype Sample_0, Coverage Sample_0, Coverage By Allele Sample_0, Variant Quality Sample_0, and Genotype Quality Sample_0?
Genotype (Sample Name) = nucleotide. Coverage (Sample Name) = will fail if there are insufficient reads. Coverage by allele (Sample Name) = will fail on one strand (+/-) read if only one side of the pair was sequenced. Variant Quality (Sample Name) = confidence of variant called. Genotype Quality (Sample Name) = confidence of genotype sequenced.
Concerning the column of "CHROM", would you let me know the rules of naming?
type of accession number| actual number| type of sequence| actual curated version used
Does your NGS service including RNA isolation?
We do not provide RNA isolation service by default. However we can provide this service. For more information, please refer to Cat#IR19001.
How many biological replicates do I need for each condition?
To increase confidence and reduce experimental error it is suggested that you submit at least 3 replicates per sample. Note that this is to serve as a guideline only and the final number of replicates and samples is to be determined by the end user based on their final experimental conditions.