Genomics Resource Library
A complete workflow from single-cell isolation to mRNA sequencing analysis white paper
This white paper examines the complete workflow of using BD FACS™ cell sorting instruments combined with BD Precise™ assays to perform single-cell gene expression analysis.
A novel method for absolute quantification of individual mRNA transcripts enables efficient characterization and validation of large-scale whole-transcriptome studies white paper
This white paper discusses a Cancer Genomics Research (CGR) study that used recently developed precision biology technologies in conjunction with next-generation sequencing (NGS) and cloud bioinformatics to characterize and validate differentially expressed candidate gene targets.
This white paper provides data on how the BD CLiC™ amplicon-AS kit connects AmpliSeq™ library prep kits with the BD CLiC platform.
Cell cycle gene expression profiling for single cancer cells using BD™ Precise mRNA kit white paper
This white paper discusses a BD study that analyzed gene expression profiles of different cell cycle states by sequencing mRNAs from single cells sorted by the BD FACSMelody cell sorter, using the BD™ Precise kit for library generation.
This white paper describes methods used to quantify the contamination potential of the BD CLiC™ platform.
This white paper describes how BD Precise™ assays use our patented Molecular Indexing (MI) technology with sample indexing to label individual mRNA transcripts and provides technical notes on MI counting and adjustment methods.
Performance of whole-genome sequencing using a titration of 2—20 ng human gDNA input into library preparation with BD CLiC™ library prep platform and KAPA HyperPlus kit white paper
This white paper examines how the BD CLiC™ platform can generate high-quality next-generation sequencing (NGS) libraries in a single run and the impact its performance on whole-genome sequencing (WGS).