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About

The Biomics Platform is the C2RT structure at Institut Pasteur for Next Generation Sequencing and includes both short and long-read technologies.

Our mission is to facilitate scientific discovery within Pasteur Institute’s network and academic research institutes. Biomics accepts both service and collaborative projects and works closely with the C3BI and DSI to provide data analysis solutions and data storage for researchers. Please contact us for pricing and turnaround times.

Our website, https://biomics.pasteur.fr, allows you to:

  • Submit a new projet
  • Ask questions (price, delay time, grants…)
  • Monitor the progress of your project
  • Information on the services provided

Here are some examples of what we propose (Procaryotes, Eukaryotes and Viruses):

  1. Technology: Short-Reads (Illumina), Long-Reads (PacBio et Nanopore)
  2. DNA-Seq: Sequencing de novo and targeted
  3. RNA-Seq: Transcriptomic Analysis
  4. Métagenomic: Targeted sequencing studies (16S, 18S, ITS) or random (Shotgun)
  5. Bioinformatics: NGS data analysis (Variant, Assembly, Methylation study…)

Biomics and its staff of experts work hard for the successful and timely processing of all samples and requests. If you are unsatisfied with our service or have a suggestion on how we can improve please do not hesitate to contact us: Reclamation / Suggestions

Members

Projects

Transversal Project

Software

Tools

Services

Training on the Agilent Bioanalyzer

A SPOC for using the Agilent Bioanalyzer Training sessions for the use of the Bioanalyzer, organized at the Transcriptome and Epigenome platform of the Biomics pole, are now replaced by a SPOC, available 24 […]

Pushing the Limit: A Complete Solution for Generating Stranded RNA-Seq Libraries from Picogram Inputs of Total Mammalian RNA

With challenging samples, like RNA isolated using laser capture microscopy, it is difficult to obtain 10 ng of starting material; additionally, rRNA depletion leads to sample loss, undermining robust library preparation. The new release surpasses […]

Index compatibility for sequencing

Illumina uses a green laser to sequence G/T and a red laser to sequence A/C. At each cycle at least one of two nucleotides for each color channel need to be read to ensure […]

Protocol for library construction available allowing to perform RNAseq from low input

The SMARTer Ultra Low Input RNA Kit for Sequencing – v3 incorporates Clontech’s patented SMART (Switching Mechanism at 5’ End of RNA Template) technology. This technology uses the template switching activity of reverse transcriptase […]

Fundings

Publications

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