What is Long Read Sequencing?
Long read sequencing, driven by advanced tech, provides continuous, extended sequences with key benefits: better genome assembly, precise structural variation ID, and full-length transcript discovery.
Our expert bioinformatics team ensures your research success. Contact UnixGene for support.
Our Bioinformatic Counseling Services
Our team of skilled bioinformatics experts understands the complexities of long read sequencing data analysis and is dedicated to assisting researchers throughout their projects. Here’s how we can help.
Data Preprocessing
We guide you through the essential steps of quality assessment, error correction, and data filtering to ensure accurate and reliable downstream analyses.
Genome Assembly
With our expertise, you can achieve robust denovo genome assemblies, leveraging the unique strengths of long read sequencing while effectively managing higher error rates.
Variant Calling and Structural Variation Analysis
Our support extends to variant calling and structural variation analysis, addressing the specific challenges posed by long read data.
Transcriptomics
Unravel the full potential of your long read RNA sequencing experiments as we help you identify complete transcripts and isoforms.
Epigenetics
Our consulting includes assistance with long read sequencing data for epigenetic studies, such as methylation analysis.
Data Integration
To provide a comprehensive understanding of your biological systems, we aid in the seamless integration of long read sequencing data with other omics datasets.