ATGENOMIX CONNECTED-READS

Accuracy

Reduce false positive and false negative in your existing resequencing analysis by eliminating mapping error and bias with assembly-to-assembly alignment.

Advanced Analytics

Detect highly accurate known and novel structural variants, and discover previously inaccessible genomic information with unrivaled data mining algorithm and de facto methodology.

Haplotyping

Allow optimal haplotype assembly from long-range sequence data for phasing analysis of disease-causing mutations.

Compatibility

Transform to scalable big-format and de facto FASTQ format compatible with the existing bioinformatics tools while featuring storage reduction.

Higher ROI

Increase the return on investment in your analysis projects by taking full advantages of NGS and reanalyzing your existing sequencing data.

And More

Drive complexity out of short-read processing to streamline new pipeline development; a wide variety of molecular diagnostic utilities can become available or more effective.

Correct

Parallel suffix-array based error detection by identifying statistically under-represented suffixes of all length and correction by the multiple manifestations of an error.

Overlap

Fast string graph-based overlap-layout-consensus method by identifying longest irreducible overlaps among reads 13X speedup over existing implementations.

Merge

Large-scale graph-processing based unitig extension by merging pairs of overlapped consensus sequences with read pair information.

Coalesce

Advanced graphical model based clustering of the contiguous sequences by coalescing around the barcode indexes of reads into long-range haplotype contigs.