De novo Analysis of DNA and RNA Genomic Data from Next Generation Sequencers to identify biomarkers.
De novo Masking of repetitive regions of DNA and RNA Reads from Next Generation Sequencers to identify biomarkers.
Graphical data visualization of genome analysis results.
Database of results from SERF analysis of Genomes.
Cluster SERF results by size, position, motif and totals
Alignment of large high-throughput sequencing reads to a reference genome
Alignment of Short Reads from Next Generation Sequencers to a Reference Genome.
Fast Alignment of Short Reads from Next Generation Sequencers to a Reference Genome.
Analytics and utilities for Variant Calling using VCF data.
Analytics and utilities for CNVs, Consensus, Annotations and other Variant Calling using VCF or BCF data.
Manipulation of read alignments including sorting, merging, indexing, retrieval of reads and Mpileups.
A high throughput Quality Control analysis of sequenced reads
Remove adapter sequences from high-throughput sequencing reads.
Transcript assembly, differential expression, and differential regulation for RNA-Seq.
Generation of sequenced reads from a reference genome with SNPs and INDEL polymorphisms.
High Performance Inline Stream Processing
Unlimited Use as Needed Scalable Servers and Storage
Use BioSerf's secure and scalable Amazon AWS cloud infrastructure to run analytics on genome datasets generated by internal or external NGS equipments. Maintain security and privacy of all analytics and results. No hardware or software to install. Access analysis tools and monitor runs using laptops, desktops or mobile devices. Web User Interface without need for Linux System or Command Line Interface knowhow enables focus on biology.
Use your institutions private secure and scalable Amazon AWS cloud infrastructure to run BioSerf analytics on genome datasets generated by onsite NGS equipment. Maintain security and privacy of all analytics and results. No hardware or software to install. Access analysis tools and monitor runs using laptops, desktops or mobile devices. Web User Interface without need for Linux System or Command Line Interface knowhow enables focus on biology.
Use your institutions private secure and scalable Amazon AWS cloud infrastructure to run BioSerf analytics on genome datasets generated by offsite NGS equipment. Maintain security and privacy of all analytics and results. No hardware or software to install. Access analysis tools and monitor runs using laptops, desktops or mobile devices. Web User Interface without need for Linux System or Command Line Interface knowhow enables focus on biology.
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