Bioinformatic Analysis of RNA-seq Total Transcriptome from low amount or low quality RNA data

0.00

Reference: S.1.13.IT.149.45
Material provided: data
Unit definition: See product page
Provider country: Italy (Polo d'Innovazione di Genomica, Genetica e Biologia - PoloGGB)

RNA-Seq is widely used to analyse the transcriptome of a cell and its changes, so allows the gene-expression profiling and the characterization of coding and non-coding transcripts to test differential expression across study groups. Total RNA-Seq analyzes both coding and multiple forms of noncoding RNA for a comprehensive view of the transcriptome.

Benefits of RNA sequencing analysis:

  • Captures both known and novel features
  • Allows to identify biomarkers across the broadest range of transcripts
  • Enables a more comprehensive understanding of phenotypes of interest
  • Allows profiling of the transcriptome across a wide dynamic range
SKU: S.1.1.IT.149.40 & S.1.6.IT.149.45-1-2 Category: Tags: ,

Description

The bioinformatic analysis service includes the following for each sample:

  • Quality control and pre-processing of raw data
  • Mapping to the genome or to the annotated transcriptome (when a reference sequence is available)
  • Transcriptome assembly (if reference genome is not available or is incomplete)
  • Differential gene expression analysis
  • Gene Set enrichment analysis
  • Data visualization including counts, PCA, volcano, and gene set enrichment dot plots (if required)

 

Material provided: data & bioinformatic analysis

Unit definition: Analysis of 800 million reads for 2×75 Paired End length (suggested at least 30 million of reads per sample – 24 samples per run).

1 Unit should allow testing at least four experimental conditions + two control conditions, with four replicates of each condition = total 24 RNA samples. Four replicates per condition are recommended. Please do not submit projects with less than three replicates per condition, which would be inadequate for statistical analysis.

 

END-USER RESPONSIBILITIES:

– DESPATCH OF DATA

  • Bioinformatic data will be shared through HD or OneDrive platform
  • The files should be labelled correctly and metadata information necessary for the analysis should be shared
  • Complete the enclosed Sample Submission form and return by email to: customer@pologgb.com.

SUPPLIER RESPONSIBILITIES:

– STORAGE OF DATA

Polo d’Innovazione Genomica Genetica Biologia waives any responsibility for the storage and backup of the supplied project and sequencing data after delivery to the end-user. Polo d’Innovazione Genomica Genetica Biologia will store the project data only for 1 month after delivery. After expiration of this period, all data are removed from our servers and archived (unless otherwise agreed with the end-user). Your data might be re-imported at an extra cost within the period of 1 year after delivery of the final data. After 1 year, all project data will be deleted permanently from our systems. Extended data storage is available on request at an extra cost and must be requested at project start.

– DELIVERY OF RESULTS

The bioinformatics results will be sent according to the Modalities of Transfer with a Bioinformatic Reports PDF Files. The bioinformatic analysis will be executed in 45 days starting from the data sharing or from the generated sequencing data.

Modalities of transfer:

  • by “WeTransfer” platform for data of up to 2Gb
  • by “MegaSync” platform for data ranging from 2Gb to 15Gb
  • by HD for data over 15 Gb

Please note that the cost of HD driver is not included. Where requested, the end-user must provide the HD.

 

For more information, please contact us.

For technical assistance, contact Polo GGB Technical Support:
Email: techsupport@pologgb.com
Telephone: 0039 0577 381310

Additional information

Provider country

Italy

Provider(s)

Polo d'Innovazione di Genomica, Genetica e Biologia (PoloGGB)

Eligibility

In order to conform to H2020 rules promoting scientific interaction between countries, if your institute is located in the provider country, you need to choose another similar product, or form a user group to request this product, Please check: http://infravec2.eu/user-groups/