Ridom SeqSphere+

Software Features


Client/server architecture

The client/server architecture allows distributed workgroups to cooperate via intra- or internet. Multiple users can access the data from various computers. Access rights and privileges can be configured to restrict access for specific users.

DNA re-sequencing editor

Assemble raw reads (FASTQ) using SKESA, Velvet, SPAdes, Flye or Raven (combined with Medaka and ONT-cgMLST-Polisher for polishing; bioRxiv), and BWA. Read and analyze assembly files (FASTA, GB, BAM, ACE). Interspecies-contamination check with Mash Screen. Edit and analyze WGS or Sanger DNA sequence data.


Editor for NGS data

Pipeline for automated sequence analysis

Define and start a pipeline to trim by quality, down-sample, assemble, analyze, and type hundreds of NGS data at once automatically; e.g. by fetching raw reads from the benchtop sequencer as soon as data are generated. Automatic read data quality and adapter content control. Define quality criteria (e.g., % of good cgMLST targets) for sample success. Correct handling of repeated samples is built-in to the pipeline.

Characterize bacteria

Type bacteria automatically with user defined QC parameters (e.g., coverage or frame shift). Genome-wide allele and SNP calling from WGS data either on core genome and/or accessory genome level is implemented. Use public schemes for genotyping or define them by using the incorporated cgMLST Target Definer. Use the NCBI AMRFinder for resistance prediction. Salmonella (SISTR), E. coli and L. monocytogenes geno-serotyping. MOB-suite and MobileElementFinder plasmid reconstruction and characterization.


Minimum Spanning Tree

Database

Store, search, retrieve, export, and create reports from experiment, circumstantial information (e.g., place, time), and DNA sequence data stored in an integrated database. Data fields are compliant with the meta-data requirements of the EBI European Nucleotide Archive (ENA). Compare new sequence entries against stored data. Get automatically clonal and/or plasmid transmission alerts of possible clusters (Microbiol Spectr. 12: e0210024, 2024). Manage and backup all data (sequence and epi-data). Download from NCBI Genome complete/draft genomes or NCBI SRA reads. Submit with just one click raw read- and epi-data to EBI ENA.


Editor for database fields

Analytical tools

Visualize place, time, 'person', and type dimensions in a comparison table with built-in GIS, epi-curve, and phylogenetic tree (among others the minimum spanning tree algorithm is supported) functionality. All dimension views are inter-linked and exportable in publication quality format (SVG and EMF). Store tree coloring, topology, and selection of samples in a comparison table snapshot. Search for group-specific SNPs, e.g., for designing a cluster specific PCR screening assay (Microbiol Spectr. 10: e0303622, 2022 [PubMed]). Visualize and compare plasmids with pyGenomeViz.


Place, time, 'person' and type dimension visualized

Community

Download certified typing schemes online. Rapidly and easily share typing schemes with others. Contribute optional to the world-wide expanding publically available cgMLST.org server of allele nomenclature. Consortium Server functionality allows several Seq-Sphere+ users each with their own installation to share a minimum agreed upon amount of data. The shared data can be used for automatically triggered matching alert (MA) emails.

Security

Encryption (SSL) of all data in transmission. Configurable anonymization of meta-data like place and time before making data public (ENA submission). Various configurable user roles, user groups and access controls. Audit trail functionality (who did, what, and when).


System Requirements

Microsoft Windows 64-bit or Linux 64-bit, quad-core processor, 16-32 GB RAM, >1 TB harddisk (depending on the amount of data that should be stored). See the SeqSphere+ documentation for more detailed system requirements.

Licensing

The license is limited to a period and a certain number of named user accounts on the server. During the license period an unlimited number of samples can be analyzed. Each named user account allows to login interactively once at the same time. If somebody else logs in with the same account, a read-only mode is activated for this session. The Pipeline Mode also runs on behalf of a named user account but can run concurrently multiple times. Client software can be installed on an unlimited number of computers. The license period starts with the activation of the license. The license will expire after the defined period and the software runs with read-only access unless a new license is ordered. Read-only access still allows to view and export existing data. Licenses include updates of SeqSphere+ and the purchased modules and free technical support for installation and troubleshooting of the software within the period. The extra charged Long-read Data Analysis Bundle (LDAB) that includes ONT Data Assembly and Long-read Data Plasmid Transmission Analysis Modules.

FOR RESEARCH USE ONLY. NOT FOR USE IN CLINICAL DIAGNOSTIC PROCEDURES.

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