How much PhiX spike in is recommended when sequencing low diversity libraries on Illumina platforms? - Illumina Knowledge
CoreGenomics: Why no PhiX on BaseSpace: %Q30 vs error rate, should you choose between them
TailorMix Dual-Indexed PhiX Control Library (Non-denatured) | SeqMatic
High-quality single amplicon sequencing method for illumina MiSeq platform using pool of 'N' (0–10) spacer-linked target specific primers without PhiX spike-in | BMC Genomics | Full Text
Dual indexed design of in-Drop single-cell RNA-seq libraries improves sequencing quality and throughput | bioRxiv
Sequencing errors in relation to coverage, minor allele count, and... | Download Scientific Diagram
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Using a PhiX Control for HiSeq Sequencing Runs - Illumina
Index mis-assignment to Illumina's PhiX control - Enseqlopedia
DNA SEQUENCING: ILLUMINA WORKFLOW PART-3 (LIBRARY NORMALIZATION, POOLING, and SEQUENCING)
Proportion of the contaminant reads that mapped to PhiX, horse and... | Download Scientific Diagram
Do my QuantSeq FWD-UMI reads look okay?
Illumina High Throughput Sequencing | DNA Technologies Core
Index mis-assignment to Illumina's PhiX control - Enseqlopedia
Run-Only Sequencing for Fast and Affordable NGS Results | Source BioScience
PhiX Control v3 - www.bio-active.co.th
3. Quality control — Genomics Tutorial 2020.2.0 documentation
Using a PhiX Control for HiSeq Sequencing Runs - Illumina
