Genomics Resource Library

White Paper

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.


Size: 132 KB
Poster

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.


Size: 2 MB
White Paper

BD CLiC™ system amplicon-AS library prep kits white paper

This white paper provides data on how the BD CLiC™ amplicon-AS kit connects AmpliSeq™ library prep kits with the BD CLiC platform.


Size: 132 KB
Poster

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.


Size: 2 MB
Poster

Contamination testing for BD CLiC™ NGS library prep under 0.1% white paper

This white paper describes methods used to quantify the contamination potential of the BD CLiC™ platform.


Size: 1 MB
White Paper

Molecular Indexing counting adjustment methods white paper

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.


Size: 132 KB
Poster

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).


Size: 132 KB

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