Gholson J. Lyon

发表

Indel variant analysis of short-read sequencing data with Scalpel

Han Fang, Vladimir Vacic, Michael C. Schatz, 2015 .

SeqMule: automated pipeline for analysis of human exome/genome sequencing data

Kai Wang, Yufeng Shen, Gholson J. Lyon, 2015, Scientific Reports.

Phen2Gene: rapid phenotype-driven gene prioritization for rare diseases

Chunhua Weng, Mengge Zhao, James M Havrilla, 2019, bioRxiv.

The Human Phenotype Ontology in 2017

Tudor Groza, Damian Smedley, Peter N. Robinson, 2016, Nucleic Acids Res..

HadoopCNV: A dynamic programming imputation algorithm to detect copy number variants from sequencing data

Gary K. Chen, Hui Yang, Max M. He, 2017, bioRxiv.

Accurate detection of de novo and transmitted INDELs within exome-capture data using micro-assembly

Michael C. Schatz, Giuseppe Narzisi, Michael Wigler, 2014, bioRxiv.

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Michael C. Schatz, Giuseppe Narzisi, Michael Ronemus, 2014 .

Human genetics and clinical aspects of neurodevelopmental disorders

Jason O'Rawe, Gholson J. Lyon, G. Lyon, 2014, bioRxiv.

"Chromosome-scale scaffolding of de novo genome assemblies based on chromatin interactions"

Han Fang, Gholson J. Lyon, G. Lyon, 2014 .

Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome

Douglas W. Woods, Jae Hoon Sul, Michael S. Okun, 2016, Neuron.

SCN8A mutation in a child presenting with seizures and developmental delays

Gholson J. Lyon, Miriam H. Meisler, J. Coppinger, 2016, Cold Spring Harbor molecular case studies.

Peptide signaling in Staphylococcus aureus and other Gram-positive bacteria

Gholson J. Lyon, Richard P. Novick, G. Lyon, 2004, Peptides.

Whole genome sequencing of one complex pedigree illustrates challenges with genomic medicine

Han Fang, David Mittelman, Gholson J. Lyon, 2017, BMC Medical Genomics.