Get Answers Faster
Rubicon Genomics PicoPLEX DNA-seq Kit creates 48 sequencing-ready libraries in less than three hours. A single kit- no other reagents needed; 48 dual barcodes included. The fastest and most cost effective method for highly reproducible aneuploidy screening and diagnosis of unbalanced inheritance of chromosome abnormalities on Illumina NGS platforms.
Reduce Contamination and Error
With PicoPLEX DNA-seq, the entire protocol is performed in a single tube or well. Purification steps don’t exist. No samples transfers are necessary. Create a sequencing-ready library from a single blastomere in 3 simple steps in less than 3 hours.