Discovery of rare mutations in extensively pooled DNA samples using multiple target enrichment

Efficient identification of rare variants in large populations: deep re-sequencing the CRP locus in the CARDIA study

(2013) Christina T. L. Chen et al.   NUCLEIC ACIDS RESEARCH

Detection of ultra-rare mutations by next-generation sequencing

(2012) M. W. Schmitt et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders

(2012) B. J. O'Roak et al.   SCIENCE

Statistical Mutation Calling from Sequenced Overlapping DNA Pools in TILLING Experiments

(2011) Victor Missirian et al.   BMC BIOINFORMATICS

Discovery of Rare Mutations in Populations: TILLING by Sequencing

(2011) H. Tsai et al.   PLANT PHYSIOLOGY

Evaluation of genomic high-throughput sequencing data generated on Illumina HiSeq and Genome Analyzer systems

(2011) André E Minoche et al.   GENOME BIOLOGY

TILLING and Associated Technologies

(2010) Trevor Wang et al.   Journal of Integrative Plant Biology

Mutation discovery by targeted genomic enrichment of multiplexed barcoded samples

(2010) Isaäc J Nijman et al.   NATURE METHODS

Target-enrichment strategies for next-generation sequencing

(2010) Lira Mamanova et al.   NATURE METHODS

Microdroplet-based PCR enrichment for large-scale targeted sequencing

(2009) Ryan Tewhey et al.   NATURE BIOTECHNOLOGY

TILLING to detect induced mutations in soybean

(2008) Jennifer L Cooper et al.   BMC PLANT BIOLOGY