NGS High Throughput Genomics Core at BRCAS
1. How do I get started working with the NGS services? (User Manual)
2. How do I fill out the forms on NGS Core LIMS?
3. How do I download my sequencing data?
4. How do I pay my fees? (Billing Procedures)
1. How to select index for illumina sequencing?
2. Index hopping issue on patterned flowcells and methods of mitigation. (NextSeq2000 / iSeq)
3. Commonly used Illumina library prep kits and protocols.
4. Illumina Adapter Sequences
5. RNA-seq data processing: HTSream and FASTP
6. Adaptor trimming for TruSeq DNA Methylation
7. Illumina PhiX control is GI:9626372 RefSeq:NC_001422.
8. Amplicon-seq design for Illumina library architecture