David E Larson

发表

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Yeting Zhang, Heng Li, Eric Banks, 2018, Nature Communications.

Using SomaticSniper to Detect Somatic Single Nucleotide Variants.

Travis E. Abbott, David E Larson, Travis E Abbott, 2014, Current protocols in bioinformatics.

svtools: population-scale analysis of structural variation

Indraniel Das, David E Larson, Ira M Hall, 2019, Bioinform..

Use of whole-genome sequencing to diagnose a cryptic fusion oncogene.

Ken Chen, Li Ding, Mark A Watson, 2011, JAMA.

Dynamic Decapentaplegic signaling regulates patterning and adhesion in the Drosophila pupal retina

David E Larson, Ross Cagan, Julia B. Cordero, 2007, Development.

Massively parallel sequencing approaches for characterization of structural variation.

Ken Chen, Li Ding, David E Larson, 2012, Methods in molecular biology.

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.

Ingo Ruczinski, Qunyuan Zhang, Ferdouse Begum, 2015, American journal of human genetics.

Exome-based mapping and variant prioritization for inherited Mendelian disorders.

Jennifer D. Churchill, David E Larson, Nathaniel G. Nutter, 2014, American journal of human genetics.

Patterns and functional implications of rare germline variants across 12 cancer types

Li Ding, Benjamin J Raphael, Benjamin J. Raphael, 2015, Nature Communications.

Clonal architecture of secondary acute myeloid leukemia.

Ken Chen, Li Ding, Xian Fan, 2012, The New England journal of medicine.

Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection

David E Larson, R. Wilson, D. Larson, 2013, Current protocols in bioinformatics.

The Caulobacter crescentus polar organelle development protein PodJ is differentially localized and is required for polar targeting of the PleC development regulator

David E Larson, Y. Brun, Yves V Brun, 2003, Molecular microbiology.

Recurring mutations found by sequencing an acute myeloid leukemia genome.

Ken Chen, Li Ding, Joshua F. McMichael, 2009, The New England journal of medicine.