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NGS Pre-Processing
Import Illumina, PacBio and NanoPore reads
Trim, filter and demultiplex both single-end and paired-end data
Merge paired reads
De-duplicate
Error correct and normalize
Filter out chimeras
Data Management
Simply drag and drop to import, export and convert your sequences, annotations and notes in common file formats including Genbank, SnapGene, FASTQ, FASTA, BAM, VCF, GFF, or import your complete Vector NTI database. Arrange and browse your data library how you like with document filtering, batch renaming, and document history automatically saved. Available for Mac, Windows and Linux.
NGS Analysis and Genomics
Workflows
Save time and ensure your work is repeatable by creating or using in-built workflows.
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