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(Discover CNV in genomes (a Matt Porter and Korf lab collaboration))
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This page summarizes the methods and data available from the Comai lab
 
This page summarizes the methods and data available from the Comai lab
  

Revision as of 17:07, 6 April 2013

Logo.png This page summarizes the methods and data available from the Comai lab

Contents

TILLING and High throughput sequencing

Custom barcoding for Illumina and Illumina barcoded reads pipeline

RESCAN: genotyping and mutation discovery

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

Heterosis

Polyploidy

Functional genomics of plant polyploids: NSF DBI 0733857

REVOLUTA legacy data

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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