Automation friendly whole exome sequencing reagents. Library prep compatible with enzymatic fragmentation. Library prep includes 192 reactions and hybridization capture includes 16 reactions (12-plex exome capture). QuantityProductCatalog #Price xGen™ DNA Library Prep EZ 96rxn10009821$2,275.00 USD ...
With the fastest run times of any benchtop next-generation sequencer, at the most affordable price, the Ion Proton Sequencer provides a simple, scalable, and affordable solution for whole exome sequencing in cancer research. Combined with theIon Chef Systemfor automated template prepar...
Whole genome sequencing (WGS) provides unprecedented access to genomic information, accelerating breakthroughs in human healthcare, oncology, biomarker discovery, agriculture, and metagenomics. Our whole genome sequencing services use cutting-edge technologies and bioinformatics to deliver high-quality data and...
Price Inquire for pricing Inquire aboutWhole Exome SequencingServices Online. Submit the adjacent Test Request Form and our laboratory will be in touch to confirm your inquiry. Note:For individuals interested in these services, please speak to your healthcare professional. ...
The first decade of capture‐based targeted whole exome sequencing (WES) has now passed, while the sequencing modality continues to find more widespread usage in clinical research laboratories and still offers an unprecedented diagnostic assay in terms of throughput, informational content and running ...
Using Next Generation Sequencing methodology, we provide sequence information that spans the complete genome, which is comprised of approximately 3.2 billion base pairs. In contrast to Whole Exome Sequencing, WGS provides sequence information spanning coding, non-coding, and intergenic regions as well ...
Price Inquire for pricing Inquire aboutWhole Exome Clinical ReportingServices Online. Submit the adjacent Test Request Form and our laboratory will be in touch to confirm your inquiry. Note:For individuals interested in these services, please speak to your healthcare professional. ...
WES: Whole-exome sequencing WGS: Whole-genome sequencing References Naghavi M, Abajobir AA, Abbafati C, Abbas KM, Abd-Allah F, Abera SF, et al. Global, regional, and national age-sex specific mortality for 264 causes of death, 1980–2016: a systematic analysis for the Global Burden ...
RNA sequencing–low-quality or low-input samples Library prep and indexing primers for automation-compatible whole transcriptome sequencing of low-quality or low-input RNA samples. QuantityProductCatalog #Price xGen™ Broad-range RNA Library Prep 96rxn10009813$3,160.00 USD ...
ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data. Nucleic Acids Res 2010;38:e164. 16. Magi A, Tattini L, Cifola I, et al. EXCAVATOR: detecting copy number variants from whole-exome sequencing data. Genome Biol 2013;14:R120. 17. Cengiz FB, ...