We’re thrilled that so many researchers around the world have published their work using Solix products. We’re in the last stage of launching our Publications Database of over 2600 articles, and hope to share it with you soon. In the meantime, check out some featured articles below.


Development and validation of a clinical cancer genomic profiling test

Characterizing and measuring bias in sequence data

Optimal enzyme for amplifying sequencing libraries

Researchers at Foundation Medicine have created a test to interrogate base substitutions, indels, copy number alterations and selected fusions across 287 cancer related genes from FFPE tumor samples using massively parallel next generation sequencing.
Researchers at the Broad Institute evaluate four sequencing platforms using human and microbial samples to assess sources of bias in sequencing and sample preparation workflow processes.
Researchers at the Sanger Center investigate many thermostable DNA polymerases along with various reaction conditions for adapter-ligated fragments for Illumina Sequencing in efforts to determine and reduce bias.