Contact us

SeqOne S.A.S

Address
SeqOne S.A.S.
22 Rue Durand
34000 Montpellier, France
Contact
Pauline
+33 (0) 9 54 40 42 84
contact@seq.one

NEW FEATURES

We are always listening to our customers and updating the SeqOne | Platform to ensure it meets your specific needs. Here are a selection of new features in the latest release of SeqOne that we hope will make your work easier and more efficient.

See how it works

IdentiCheck

Verifies that each sample analyzed corresponds to the right patient. Reduces the risk of delivering the wrong results due to samples being swapped or mislabeled.

Gene Coverage

Provides detailed information on sequencing coverage of each gene making it possible to assess the quality of sequencing. Gene Coverage reduces the risk of interpretation errors linked to sequencing or wetlab errors.

Quality Report

A detailed A detailed quality report with configurable triggers that flag any sequencing parameter that falls below your minimum standard. Used in conjunction with Gene Coverage, you can inspect areas that have been flagged in the Quality Report to decide whether it is best to re-sequence the sample or to proceed with the interpretation.

Application catalog

A series of vertical bioinformatic application each specifically designed to address a particular genomics analysis challenge
> Read more

Local Info Sync (LIS)

Local Info Sync is a piece of software that installs on a virtual machine in your network and manages all data transfers between SeqOne and your local data stores. LIS automates the transfer of data from the sequencer and your local LIMS and patient management system. It also makes it possible to select Worksets and launch analyses dramatically reducing the time lost in data manipulation.

Variant knowledge base (VKB)

Share information on variants annotated by other members of your team or other teams. VKB provides a great way to collaborate on interpretation while giving you total control of which data you share and which you keep private.

HPO code support

Rank variants more precisely by using HPO information to improve the efficiency of the AI ranking algorithm and speed identification of causal variants. Using HPO-enhanced ranking causal variants will be identified much more reliably reducing time and errors in your process.

IdentiCheck

Verifies that each sample analyzed corresponds to the right patient. Reduces the risk of delivering the wrong results due to samples being swapped or mislabeled.

Gene Coverage

Provides detailed information on sequencing coverage of each gene making it possible to assess the quality of sequencing. Gene Coverage reduces the risk of interpretation errors linked to sequencing or wetlab errors.

Quality Report

A detailed A detailed quality report with configurable triggers that flag any sequencing parameter that falls below your minimum standard. Used in conjunction with Gene Coverage, you can inspect areas that have been flagged in the Quality Report to decide whether it is best to re-sequence the sample or to proceed with the interpretation.

Application catalog

A series of vertical bioinformatic application each specifically designed to address a particular genomics analysis challenge
> Read more

Local Info Sync (LIS)

Local Info Sync is a piece of software that installs on a virtual machine in your network and manages all data transfers between SeqOne and your local data stores. LIS automates the transfer of data from the sequencer and your local LIMS and patient management system. It also makes it possible to select Worksets and launch analyses dramatically reducing the time lost in data manipulation.

Variant knowledge base (VKB)

Share information on variants annotated by other members of your team or other teams. VKB provides a great way to collaborate on interpretation while giving you total control of which data you share and which you keep private.

HPO code support

Rank variants more precisely by using HPO information to improve the efficiency of the AI ranking algorithm and speed identification of causal variants. Using HPO-enhanced ranking causal variants will be identified much more reliably reducing time and errors in your process.

Next generation genomic analysis for next generation healthcare