NGS Pre-Processing, Mapping and De Novo Assembly
Import any data type, demultiplex, trim, filter, assemble or map to reference.
Extensive Pre-Processing of Sequencing Reads
Clean sequence data is critically important for accurate downstream analysis. Make sure your data is in tip-top shape by taking advantage of easy access to all of the necessary pre-processing tools:
- Demultiplex/split by barcode
- Trim and filter by read quality
- Trim adapters
- Merge paired reads
- De-duplicate
- Error correct and normalize
- Filter out chimeras
Reliable Reference Mapping
The exclusive Geneious Read mapper with its iterative approach produces superior results when compared to other popular mapping algorithms and can correctly align structural variants. If you need something a bit different, Bowtie, TopHat and BBMap are all at your fingertips.
Flexible De Novo Genome Assembly
The Geneious Assembler is flexible enough to handle data from any type of sequencing machine with reads of any length, including paired-reads and mixtures of reads from different sequencing machines. It’s particularly good for microbial assemblies with the unique capability to produce circular contigs. Alternatively, running MIRA, SPAdes, Tadpole or Velvet is just as easy, and MAUVE genome alignment is on hand to help you with genome comparison and finishing.
Resources
VIDEOS
EXPLORE GENEIOUS PRIME
NGS Visualization and Analysis
Comprehensive analysis of data, including genome browser, contig visualization, SNP calling, and RNA-Seq expression analysis.
Sanger Sequencing
Trim, assemble, and view Sanger sequencing trace files. Powerful SNP detection and variant calling.
DNA Sequence Alignment
Sequence alignment, visualization and editing. Select from multiple algorithms including Clustal Omega, MUSCLE and MAFFT.
Import Data
Import and convert common file types as well as their annotations and notes with a simple drag and drop
GENEIOUS ACADEMY
