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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
672018
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
392009
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
352013
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
262017
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
242021
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
242014
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
172014
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
152019
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
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
eP443: 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, ...
Genetics in Medicine 24 (3), S278, 2022
2022
Copy number variant caller
SH HONG, P KALETA, GJ Hogan
US Patent App. 17/111,272, 2021
2021
664 High-throughput fetal-fraction amplification increases analytical performance of noninvasive prenatal screening
D Muzzey, N Welker, A Lee, R Kjolby, H Wan, M Theilmann, D Jeon, ...
American Journal of Obstetrics & Gynecology 224 (2), S417-S418, 2021
2021
High-Throughput Fetal-Fraction Amplification Increases Analytical Performance of Noninvasive Prenatal Screening
D Muzzey, N Welker, A Lee, R Kjolby, H Wan, M Theilmann, D Jeon, ...
JOURNAL OF MOLECULAR DIAGNOSTICS 22 (11), S8-S8, 2020
2020
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