# NGS data analysis

Merge paired-end Illumina sequencing reads from raw fastq files, collapse UMIs, cluster sequences and analyze enrichment

## Scalable and fast NGS analysis software

### Analyze antibody libraries and immune repertoires

#### Tools for data analysis on PipeBio

- Import Fastq files and preprocess the data by merging paired-end reads
- Collapse UMIs and use PCR error correction for accurate identification of antibody clones
- Cluster multiple samples across experiments, identify homologous clonal groups
- Calculate fold change and enrichment from immunization or biopanning experiments

#### Analyze large datasets fast

- Analyze millions of sequences in parallel and obtain results quickly
- Visualize and explore your data with intuitive charts

#### Wide support for sequencing platforms

- Illumina sequencing, including MiSeq, NextSeq, NovaSeq
- Oxford Nanopore long read sequencing
- Parse Biosciences [Single Cell Sequencing](https://www.parsebiosciences.com/)
- 10x Genomics, Single Cell barcoded sequences
- PacBio long read sequencing