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Cell Systems|December 12, 2017
Quantitative Missense Variant Effect Prediction Using Large-Scale Mutagenesis DataVanessa E Gray, Ronald J Hause, Jens Luebeck, et al.Genome Medicine|October 27, 2009
Next generation sequence analysis for mitochondrial disordersValeria Vasta, Sarah B Ng, Emily H Turner, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|April 19, 2014
Detection of minimal residual disease in NPM1-mutated acute myeloid leukemia by next-generation sequencingStephen J Salipante, Jonathan R Fromm, Jay Shendure, et al.Cell|January 16, 2016
Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-OriginMatthew W Snyder, Martin Kircher, Andrew J Hill, et al.Nature Methods|January 19, 2010
Parallel, tag-directed assembly of locally derived short sequence readsJoseph B Hiatt, Rupali P Patwardhan, Emily H Turner, et al.Bioinformatics (Oxford, England)|May 29, 2014
MIPgen: optimized modeling and design of molecular inversion probes for targeted resequencingEvan A Boyle, Brian J O'Roak, Beth K Martin, et al.Nature|August 21, 2014
Saturation editing of genomic regions by multiplex homology-directed repairGregory M Findlay, Evan A Boyle, Ronald J Hause, et al.Biorxiv : the Preprint Server for Biology|November 28, 2023
Identification of Cellular Interactions in the Tumor Immune Microenvironment Underlying CD8 T Cell ExhaustionChristopher Klocke, Amy Moran, Andrew Adey, et al.BMC Genomics|July 7, 2011
Exome-wide DNA capture and next generation sequencing in domestic and wild speciesTed Cosart, Albano Beja-Pereira, Shanyuan Chen, et al.Nature Biotechnology|November 17, 2009
High-resolution analysis of DNA regulatory elements by synthetic saturation mutagenesisRupali P Patwardhan, Choli Lee, Oren Litvin, et al.Pageof 43