Lexogen Bioinformatics Service
Next-generation sequencing (NGS) technologies are invaluable in academic research, biotechnology, biomedical and clinical research, and the pharmaceutical industry. As NGS technologies rapidly expand and develop, it is imperative to correctly interpret increasingly complex data sets and relate them to biological functions. More than ever, it is necessary to approach NGS data analysis with tailored and creative data analysis workflows to extract the most from the datasets obtained.
Our team consists of genomic data analysis experts with experience in various NGS data analysis pipelines who are passionate about developing novel, customized workflows and solutions while keeping biology at the forefront.
We speak your language, so focus on your research and leave the data analysis to us.
Benefits
- Individual approach: We approach your data with full dedication to extract all the valuable information and make sure you get the most from your experiments.
- Customization and Development: We tailor and/or develop data analysis pipelines to meet your project needs.
- Proficiency: We are genomics data analysis experts with experience in diverse data analysis pipelines and approaches.
- Data Protection: We operate under the European Union Regulation - GDPR, follow ISO27001 principles, and employ various measures to ensure the highest level of data security.
- Continuous support: You will benefit from our expertise before, during and also after the project is completed. We are always there for you.
Our Portfolio
We have extensive experience in handling diverse genomic data analysis pipelines, including various types of RNA-Seq data analysis, DNA-Seq data analysis or epigenetics. Indeed, we can adapt and customize pipelines specifically to your project needs or even develop a new data analysis pipeline for you.
Not sure which approach is the best to analyze your data, or none of the applications listed fit your goals? Get in touch with us at services@lexogen.com to schedule a free consultation!
Differential Gene Expression analysis
Functional enrichment analysis
Transcriptome assembly
Small RNA data analysis
Alternative splicing analysis
Circular RNA analysis
Alternative polyA site analysis
Internal priming filtering
Shape-Seq
ChIP-Seq
ATAC-Seq
Germline and somatic variant calling
Single-cell RNA-Seq Analysis (10x and proprietary Luthor technology)
SLAMseq data analysis
Whole-exome and whole-genome sequencing
De-novo genome assembly
Primer design for rRNA depletion
Total RNA is comprised of large amounts of ribosomal RNA (rRNA) which can make up between ~80 – 98 % of all RNA molecules in a sample. rRNA depletion removes these undesired transcripts to access transcripts of interest. If you work with less common species and struggle with rRNA depletion for your RNA-Seq experiment, we offer the primer design using our proprietary advanced algorithm.
None of the enlisted analyses fit your needs? Consult with us at services@lexogen.com for Custom Data Analysis.
Data output
Depends on your project.
All data outputs will be outlined in the offer you will receive from us after Introductory Consultations.