Custom analysis
- Comparative genomics
- Functional genomic
- Data Integration
Variation calling
- SNPs and InDELs calling
- Structural Variant calling
- PAVs and CNVs calling
Population studies
- QTLseq analysis
- GBS analysis
- Association studies and GWAS
Resequencing
- Reference Guided Assembly
- Genome reconstruction
- Marker development
Selective Sequencing
- Sequence capture analysis
- Exome analysis
- Gene panel analysis
De novo
- De novo Assembly
- Structural gene annotation
- Functional gene annotation
What can you expect from us
Genomics expertise
The genome and its correct assembly is the starting point for any project that uses omics sciences to achieve a breakthrough in the fields of human health, agriculture and the environment. For this reason, at Sequentia we develop innovative tools that create a new reliable and precise assembly, of both complete genomes and specific parts or groups of genes.
The era of low-cost mass sequencing has opened the way to resequencing techniques that allow us to study variations between individuals and related species through approaches such as genome variance. The integration of reference genomes and resequencing data has led us to design a specific tool for Reference Guided Assembly and genome reconstruction, thus creating custom versions of each subject.
We also offer gene panel analysis services or sequence capture experiments to search for variants and use our tool to reconstruct the private sequence of genes or sequenced parts.
We carry out studies on QTLseq, GBS, GWAS and comparative genomics. We offer innovative solutions for data integration, and create software solutions to independently store, display and integrate the analysis.
Integrated project management
from experiment design to data interpretation
High data privacy and security
Secure your data
Curated output
To quickly reach the scientific goal
Fast production
Quick production of results
Private IT
Private IT infrastructure and cloud systems
Custom workflows
Customise your project
Up-to-date scientific knowledge
We update continuously
Mixed methods
A mixed approach of unique well-referenced and published bioinformatics
RELATED CLOUD SOFTWARE
GINO is a user-friendly, accurate, fast and scalable software that boosts the exploitation of genomics data. It performs automated variant analysis and interpretation, working with NGS data from targeted sequencing, Whole Exome Sequencing and Whole Genome Sequencing.
GINO features customised variant filtering, virtual panels generation, trios analysis and can analyze both germline and somatic variants. It automatically generates curated reports adapted to its user’s desired outputs. GINO is a cloud-based software, allowing its users to access from any point and avoiding the need of large computational infrastructures.
GINO can answer several questions, such as:
- Which variants are present in a given individual?
- Which variants are likely to be pathogenic?
- What is the probability of inheriting a pathogenic variant?
