Kirk C. Wilhelmsen

发表

ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data

Joel S. Parker, J. S. Marron, Matthew D. Wilkerson, 2012, BMC Bioinformatics.

SMNN: Batch Effect Correction for Single-cell RNA-seq data via Supervised Mutual Nearest Neighbor Detection

Yuchen Yang, Yin Shen, Gang Li, 2019, bioRxiv.

Clinical Genomics: How Much Data is Enough?

Karamarie Fecho, Ashok Krishnamurthy, Stanley C. Ahalt, 2015 .

MaPSeq, A Service-Oriented Architecture for Genomics Research within an Academic Biomedical Research Institution

Stanley C. Ahalt, John McGee, Charles Schmitt, 2015, Informatics.

Genetics and population analysis Simulating association studies : a data-based resampling method for candidate regions or whole genome scans

Fred A. Wright, Patrick F. Sullivan, Xiaojun Guan, 2007 .

Visual Analytics to Optimize Patient-Population Evidence Delivery for Personalized Care

Kenneth Gersing, Charles Schmitt, Igor Akushevich, 2013, BCB.

Data-driven approaches to augment clinical decision in EMR Era

Stanley C. Ahalt, Kenneth Gersing, Charles Schmitt, 2012, 2012 3rd International Workshop on Cognitive Information Processing (CIP).

Batch correction of high-dimensional data

David B. Dunson, Emanuele Aliverti, Kirk C. Wilhelmsen, 2019 .

Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

Kimberly Robasky, Bradford C. Powell, Yun Li, 2021, BMC Bioinformatics.

ANTIPSYCHOTIC-INDUCED VACUOUS CHEWING MOVEMENTS AND EXTRAPYRAMIDAL SIDE-EFFECTS ARE HIGHLY HERITABLE IN MICE

Patrick F. Sullivan, Howard L. McLeod, Molly A. Bogue, 2010, The Pharmacogenomics Journal.

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2020, Nature Communications.

Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q

Stanley Fahn, Kirk C. Wilhelmsen, Daniel E. Weeks, 1993, Nature Genetics.

A New Framework and Prototype Solution for Clinical Decision Support and Research in Genomics and Other Data-intensive Fields of Medicine

Stanley C. Ahalt, Karamarie Fecho, Jonathan Berg, 2016, EGEMS.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .