Related Experiment Video
Updated: May 31, 2026

Isolation and Quantification of Axonal mRNAs Using Porous Membrane Inserts and RTddPCR
Published on: February 6, 2026
Primer PICKR: literature-mined scoring platform for robust RT-qPCR primers
Thomas G Molley1,2, Abhinaba Banerjee1,2, Alis Balayan2,3
1Shu Chien-Gene Lay Department of Bioengineering, University of California, San Diego, La Jolla, CA, USA.
None:
Reliable reverse-transcription quantitative PCR (RT-qPCR) depends on well-designed primers, yet undocumented or poorly validated sequences continue to compromise reproducibility. Existing resources catalog only modest sets of empirically verified primers or generate de-novo primer pairs without experimental validation. Here, we introduce Primer PICKR (Publication Integrations for Composite Knowledge Ranking), a large-scale, open, continuously updated database that systematically converts >7,000,000 community-validated oligonucleotides from >400,000 papers into actionable design resources. PICKR aligns sequences to reference transcriptomes and assembles ranked primer pairs for over 6000 genes across ten model organisms. Composite scoring integrates citation frequency, biophysical quality, and primer-pair synergy, while experimental validation of 154 human primer pairs spanning the score distribution demonstrates near-perfect amplification success above a PICKR score of 80. By converting decades of scattered primer choices into an immediately searchable database, Primer PICKR reduces empirical screening, conserves scarce samples, and accelerates reproducible assay development.
More Related Videos
11:13Enrichment of Native Lipoprotein Particles with microRNA and Subsequent Determination of Their Absolute/Relative microRNA Content and Their Cellular Transfer Rate
Published on: May 9, 2019
12:37Efficient Nucleic Acid Extraction and 16S rRNA Gene Sequencing for Bacterial Community Characterization
Published on: April 14, 2016