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The BRC Genomics Research Platform offers the following library preparation services for Illumina Sequencing.

The BRC Genomics Research Platform offers the following library preparation services for Illumina Sequencing.

  1. Whole Exome Sequencing  (3ug  / 200ng input)
  2. Custom Capture Sequencing (3ug  / 200ng input)
  3. Haloplex Custom Capture Sequencing
  4. Haloplex HS Custom Capture Sequencing
  5. RNASeq-Whole Transcriptome Sequencing (stranded)
  6. Small RNA Sequencing
  7. Whole Genome Sequencing
  8. BS Seq – Whole Genome Sequencing after Bisulfite conversion
  9. FFPE DNA Whole Genome Sequencing
  10. FFPE RNASeq – Whole Transcriptome Sequencing (stranded)
  11. Microbiome Sequencing
  12. 16S sequencing with V3-V4 reagents

To reduce sample to sample variation introduced through manual handling, we endeavour to prepare libraries on our Agilent Bravo liquid handling system or our Labcyte liquid handling system.

We are interested in actively developing new protocols for various applications according to your requirements. These projects are conducted as pilot projects aimed towards new technology implementation in our lab.

Please contact Dr. Alka Saxena if you wish to discuss a standard service or a pilot project with us.