Methods

This page summarizes the methods available from the Comai lab


TILLING and High throughput sequencing

Custom barcoding for Illumina and Illumina barcoded reads pipeline

Genotyping and Mutation Discovery

Exome capture: genotyping and mutation discovery

Discover CNV in genome (a Matt Porter and Korf lab collaboration)

Funding

This page and the connected tools are funded by:

  • NSF Plant Genome grant DBI-0733857 (Functional Genomics of Polyploids)
  • NSF Plant Genome grant DBI-0924025. Heterosis Challenge Grant (HCG):The Regulatory Disruption Hypothesis for Heterosis
  • NSF Plant Genome grant DBI-0822383 (“TILLING by Sequencing”)
  • National Institutes of Health R01 GM076103-01A1 (Dosage dependent regulation in hybridization) to LC.
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