关注
David Benjamin
David Benjamin
The Broad Institute
在 broadinstitute.org 的电子邮件经过验证
标题
引用次数
引用次数
年份
Calling somatic SNVs and indels with Mutect2
D Benjamin, T Sato, K Cibulskis, G Getz, C Stewart, L Lichtenstein
BioRxiv, 861054, 2019
4262019
Mitochondrial DNA variation across 56,434 individuals in gnomAD
KM Laricchia, NJ Lake, NA Watts, M Shand, A Haessly, L Gauthier, ...
Genome research 32 (3), 569-582, 2022
672022
Friedel oscillations as a probe of fermionic quasiparticles
EG Dalla Torre, D Benjamin, Y He, D Dentelski, E Demler
Physical Review B 93 (20), 205117, 2016
482016
Single-Band Model of Resonant Inelastic X-Ray Scattering by Quasiparticles in High- Cuprate Superconductors
D Benjamin, I Klich, E Demler
Physical review letters 112 (24), 247002, 2014
472014
Quantification of somatic mutation flow across individual cell division events by lineage sequencing
Y Brody, RJ Kimmerling, YE Maruvka, D Benjamin, JJ Elacqua, ...
Genome research 28 (12), 1901-1918, 2018
302018
Variational polaron method for Bose-Bose mixtures
D Benjamin, E Demler
Physical Review A 89 (3), 033615, 2014
302014
Exploring quasiparticles in high-Tc cuprates through photoemission, tunneling, and x-ray scattering experiments
EG Dalla Torre, Y He, D Benjamin, E Demler
New Journal of Physics 17 (2), 022001, 2015
232015
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data
M Babadi, JM Fu, SK Lee, AN Smirnov, LD Gauthier, M Walker, ...
Nature genetics 55 (9), 1589-1597, 2023
202023
Microscopic theory of resonant soft-X-ray scattering in materials with charge order: The example of charge stripes in high-temperature cuprate superconductors
D Benjamin, D Abanin, P Abbamonte, E Demler
Physical review letters 110 (13), 137002, 2013
192013
Calling somatic snvs and indels with mutect2. BioRxiv. 2019: 861054
D Benjamin, T Sato, K Cibulskis, G Getz, C Stewart, L Lichtenstein
View Article, 0
17
GATK-gCNV: a rare copy number variant discovery algorithm and its application to exome sequencing in the UK biobank
M Babadi, JM Fu, SK Lee, AN Smirnov, LD Gauthier, M Walker, ...
bioRxiv, 2022.08. 25.504851, 2022
92022
GATK CNV: copy-number variation discovery from coverage data
M Babadi, DI Benjamin, SK Lee, A Smirnov, A Chevalier, L Lichtenstein, ...
Cancer Research 77 (13_Supplement), 3580-3580, 2017
82017
Probing competing and intertwined orders with resonant inelastic x-ray scattering in the hole-doped cuprates
D Benjamin, I Klich, E Demler
Physical Review B 92 (3), 035151, 2015
82015
Calling somatic SNVs and indels with Mutect2. 2019; bioRxiv doi: 02 December 2019, preprint: not peer reviewedhttps
D Benjamin, T Sato, K Cibulskis, G Getz, C Stewart, L Lichtenstein
doi. org/10.1101/861054, 0
6
A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysis
M Shand, J Soto, L Lichtenstein, D Benjamin, Y Farjoun, Y Brody, ...
Communications Biology 3 (1), 744, 2020
52020
Calling Somatic SNVs and Indels with Mutect2. bioRxiv, 861054 (2019)
D Benjamin, T Sato, K Cibulskis, G Getz, C Stewart, L Lichtenstein
Acknowledgments: We thank all members of the Jan Vijg’s laboratory for …, 0
5
Pair HMM probabilistic realignment in HaplotypeCaller and Mutect
D Benjamin
Broad Institute. Available online: https://github. com/broadinstitute/gatk …, 2018
42018
GATK ACNV: allelic copy-number variation discovery from SNPs and coverage data
A Chevalier, L Lichtenstein, A Smirnov, SK Lee, M Babidi, DI Benjamin, ...
Cancer Research 77 (13_Supplement), 3581-3581, 2017
32017
Superconducting pairing in resonant inelastic x-ray scattering
Y Shi, D Benjamin, E Demler, I Klich
Physical Review B 94 (9), 094516, 2016
32016
GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data (Aug, 10.1038/s41588-023-01449-0, 2023)
M Babadi, JM Fu, SK Lee, AN Smirnov, LD Gauthier, M Walker, ...
NATURE GENETICS, 2024
2024
系统目前无法执行此操作,请稍后再试。
文章 1–20