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Citations for Illumina :

1051 - 1052 of 1052 citations for Recombinant Human TNFSF11 Fc tagged since 2019

Citations are collected from bioRxiv only, the total number of publications could be much larger.

Functional characterization of RELN missense mutations involved in recessive and dominant forms of Neuronal Migration Disorders

Martina Riva, et al., bioRxiv - Neuroscience 2021

Quote: ... using Agilent SureSelectXT Clinical Research Exome (SureSelectXT Human All Exon V5 baited with clinically relevant genes) and the Illumina NextSeq 550 sequencer (Illumina, Inc., San Diego, CA, USA) according to the manufacturer’s protocol.
The Entwined African and Asian Genetic Roots of the Medieval Peoples of the Swahili Coast

Esther S. Brielle, et al., bioRxiv - Genetics 2022

Quote: ... Ancient individuals and present-day individuals (most genotyped on the HO SNP array, and some also genotyped on the Illumina Human Omni5 Bead Chip [28]) were projected into the three-dimensional (3D ...

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