FixItFelix: improving genomic analysis by fixing reference errors
Sairam Behera(Baylor College of Medicine), Fritz J. Sedlazeck(Baylor College of Medicine), Peter Orchard(University of Michigan), Stephen C.J. Parker(Unknown), Justin M. Zook(National Cancer Institute), Daniela C. Soto(University of California, Davis), Megan Y. Dennis(University of California System), Jesse Farek(Baylor College of Medicine), Jonathon LeFaive(University of Michigan), Luis F. Paulin(Baylor College of Medicine), Albert V. Smith(University of Iceland), Medhat Mahmoud(Baylor College of Medicine)
Cited by 26
Related Papers
A second generation human haplotype map of over 3.1 million SNPs
|Nature|2007|4.6k
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome
|Nature Biotechnology|2019|2k
Genome-wide association study of blood pressure and hypertension
|Nature Genetics|2009|1.4k