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Kevin R. Haas
Kevin R. Haas
Chief Technology Officer, Myriad Genetics
Verified email at berkeley.edu - Homepage
Title
Cited by
Cited by
Year
Validation of an expanded carrier screen that optimizes sensitivity via full-exon sequencing and panel-wide copy number variant identification
GJ Hogan, VS Vysotskaia, KA Beauchamp, S Seisenberger, PV Grauman, ...
Clinical chemistry 64 (7), 1063-1073, 2018
722018
Reaction path optimization with holonomic constraints and kinetic energy potentials
JB Brokaw, KR Haas, JW Chu
Journal of Chemical Theory and Computation 5 (8), 2050-2061, 2009
402009
Expectation-maximization of the potential of mean force and diffusion coefficient in Langevin dynamics from single molecule FRET data photon by photon
KR Haas, H Yang, JW Chu
The Journal of Physical Chemistry B 117 (49), 15591-15605, 2013
372013
High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening
NC Welker, AK Lee, RAS Kjolby, HY Wan, MR Theilmann, D Jeon, ...
Genetics in Medicine 23 (3), 443-450, 2021
282021
Development and validation of a 36-gene sequencing assay for hereditary cancer risk assessment
VS Vysotskaia, GJ Hogan, GM Gould, X Wang, AD Robertson, KR Haas, ...
PeerJ 5, e3046, 2017
272017
Trajectory entropy of continuous stochastic processes at equilibrium
KR Haas, H Yang, JW Chu
The Journal of Physical Chemistry Letters 5 (6), 999-1003, 2014
252014
Fisher information metric for the Langevin equation and least informative models of continuous stochastic dynamics
KR Haas, H Yang, JW Chu
The Journal of chemical physics 139 (12), 2013
222013
Decomposition of energy and free energy changes by following the flow of work along reaction path
K Haas, JW Chu
The Journal of chemical physics 131 (14), 2009
212009
Analysis of trajectory entropy for continuous stochastic processes at equilibrium
KR Haas, H Yang, JW Chu
The Journal of Physical Chemistry B 118 (28), 8099-8107, 2014
182014
Software-assisted manual review of clinical next-generation sequencing data: an alternative to routine Sanger sequencing confirmation with equivalent results in> 15,000 …
D Muzzey, S Kash, JI Johnson, LM Melroy, P Kaleta, KA Pierce, K Ready, ...
The Journal of Molecular Diagnostics 21 (2), 296-306, 2019
162019
Next-generation sequencing assay accurately determines carrier status for spinal muscular atrophy
X Wang, HY Wan, CB Oyolu
ASHG annual meeting, 2015
22015
Software-assisted manual review of clinical NGS data: an alternative to routine Sanger sequencing confirmation with equivalent results in> 15,000 hereditary cancer screens
D Muzzey, S Kash, JI Johnson, LM Melroy, P Kaleta, KA Pierce, K Ready, ...
bioRxiv, 305011, 2018
12018
Development and validation of an expanded carrier screen that optimizes sensitivity via full-exon sequencing and panel-wide copy-number-variant identification
GJ Hogan, VS Vysotskaia, S Seisenberger, PV Grauman, KA Beauchamp, ...
bioRxiv, 178350, 2017
12017
Noninvasive prenatal screening using dynamic iterative depth optimization with depth-scaled variance determination
DE Muzzey, JR Tratner, KM D'Auria
US Patent 12,020,779, 2024
2024
Evaluation and improvement of genetic screening tests using receiver operating characteristic curves
KA Beauchamp
US Patent App. 18/592,076, 2024
2024
Bayesian sex caller
A Lee, K Haas, K D'auria
US Patent App. 18/020,416, 2024
2024
Copy number variant caller
X Wang, PV GRAUMAN
US Patent App. 17/554,721, 2022
2022
Deep learning based variant calling using machine learning
S Hong, K Beauchamp, K Haas
US Patent App. 17/039,826, 2022
2022
Fetal fraction amplification within NIPS enables detection of clinically relevant genome-wide copy-number-variants to 1Mb resolution
A Acevedo, S Cox, H LaBreche, M Alfaro, S Pierson, S Hancock, K Moyer, ...
American Journal of Obstetrics & Gynecology 226 (1), S433, 2022
2022
Copy number variant caller
SH HONG, P KALETA, GJ Hogan
US Patent App. 17/111,272, 2021
2021
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