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Dive into the research topics where Rachel Barry is active.

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Featured researches published by Rachel Barry.


Physical Review E | 2004

Local jamming via penetration of a granular medium.

Matthew Stone; Rachel Barry; David P. Bernstein; M. D. Pelc; Y. K. Tsui; P. Schiffer

We present a series of measurements examining the penetration force required to push a flat plate vertically through a dense granular medium, focusing in particular on the effects of the bottom boundary of the vessel containing the medium. Our data demonstrate that the penetration force near the bottom is strongly affected by the surface properties of the bottom boundary, even many grain diameters above the bottom. Furthermore, the data indicate an intrinsic length scale for the interaction of the penetrating plate with the vessel bottom via the medium. This length scale, which corresponds to the extent of local jamming induced by the penetrating plate, has a square root dependence both upon the plate radius and the ambient granular stress near the bottom boundary, but it is independent of penetration velocity and grain diameter.


Nature Communications | 2017

Scalable whole-exome sequencing of cell-free DNA reveals high concordance with metastatic tumors

Viktor A. Adalsteinsson; Gavin Ha; Samuel S. Freeman; Atish D. Choudhury; Daniel G. Stover; Heather A. Parsons; Gregory Gydush; Sarah C. Reed; Denisse Rotem; Justin Rhoades; Denis Loginov; Dimitri Livitz; Daniel Rosebrock; Ignaty Leshchiner; Jaegil Kim; Chip Stewart; Mara Rosenberg; Joshua M. Francis; Cheng-Zhong Zhang; Ofir Cohen; Coyin Oh; Huiming Ding; Paz Polak; Max Lloyd; Sairah Mahmud; Karla Helvie; Margaret S. Merrill; Rebecca A. Santiago; Edward P. O’Connor; Seong Ho Jeong

Whole-exome sequencing of cell-free DNA (cfDNA) could enable comprehensive profiling of tumors from blood but the genome-wide concordance between cfDNA and tumor biopsies is uncertain. Here we report ichorCNA, software that quantifies tumor content in cfDNA from 0.1× coverage whole-genome sequencing data without prior knowledge of tumor mutations. We apply ichorCNA to 1439 blood samples from 520 patients with metastatic prostate or breast cancers. In the earliest tested sample for each patient, 34% of patients have ≥10% tumor-derived cfDNA, sufficient for standard coverage whole-exome sequencing. Using whole-exome sequencing, we validate the concordance of clonal somatic mutations (88%), copy number alterations (80%), mutational signatures, and neoantigens between cfDNA and matched tumor biopsies from 41 patients with ≥10% cfDNA tumor content. In summary, we provide methods to identify patients eligible for comprehensive cfDNA profiling, revealing its applicability to many patients, and demonstrate high concordance of cfDNA and metastatic tumor whole-exome sequencing.Identifying the mutational landscape of tumours from cell-free DNA in the blood could help diagnostics in cancer. Here, the authors present ichorCNA, software that quantifies tumour content in cell free DNA, and they demonstrate that cell-free DNA whole-exome sequencing is concordant with metastatic tumour whole-exome sequencing.


Nature | 2004

Stress propagation: Getting to the bottom of a granular medium

Matthew Stone; David P. Bernstein; Rachel Barry; M. D. Pelc; Yee-Kin Tsui; P. Schiffer

Penetration by an object through a dense granular medium (for example, by a finger pushing slowly into the sand on a beach) presents an interesting physics problem that is closely related to issues of practical importance in soil science. Here we measure the penetration-resistance force for an object approaching the solid bottom boundary of a granular sample — analogous to the finger approaching a flat rock buried in the beach. We find that the penetration resistance near the boundary increases exponentially, which demonstrates the existence of an intrinsic length scale to the ‘jamming’ caused by a locally applied stress.


Proceedings of the National Academy of Sciences of the United States of America | 2016

Longitudinal multiparameter assay of lymphocyte interactions from onset by microfluidic cell pairing and culture

Burak Dura; Mariah M. Servos; Rachel Barry; Hidde L. Ploegh; Stephanie K. Dougan; Joel Voldman

Significance Many immune responses are mediated by direct cell–cell interactions and develop over multiple timescales. A mechanistic understanding of how diverse outcomes arise during these interactions entails identifying the relationships between various responses occurring at different stages by correlated measurements. Typical approaches that rely on population-wide correlations, however, reveal these connections broadly and mask the fine details that might be discernible only at the single-cell level. Here, we present a microfluidics-based cell–cell interaction assay that allows defined generation, real-time imaging, and longitudinal assay of lymphocyte interactions, thereby permitting direct correlative studies within each single cell. Our studies using this platform indicate a possible role for the strength of calcium signaling in selective regulation of cytotoxicity and interferon-gamma production of natural killer cells. Resolving how the early signaling events initiated by cell–cell interactions are transduced into diverse functional outcomes necessitates correlated measurements at various stages. Typical approaches that rely on bulk cocultures and population-wide correlations, however, only reveal these relationships broadly at the population level, not within each individual cell. Here, we present a microfluidics-based cell–cell interaction assay that enables longitudinal investigation of lymphocyte interactions at the single-cell level through microfluidic cell pairing, on-chip culture, and multiparameter assays, and allows recovery of desired cell pairs by micromanipulation for off-chip culture and analyses. Well-defined initiation of interactions enables probing cellular responses from the very onset, permitting single-cell correlation analyses between early signaling dynamics and later-stage functional outcomes within same cells. We demonstrate the utility of this microfluidic assay with natural killer cells interacting with tumor cells, and our findings suggest a possible role for the strength of early calcium signaling in selective coordination of subsequent cytotoxicity and IFN-gamma production. Collectively, our experiments demonstrate that this new approach is well-suited for resolving the relationships between complex immune responses within each individual cell.


Physical Review E | 2006

Flux through a hole from a shaken granular medium

Ke Chen; Matthew Stone; Rachel Barry; M. Lohr; W. McConville; K. Klein; B. L. Sheu; A. J. Morss; T. Scheidemantel; P. Schiffer

We have measured the flux of grains from a hole in the bottom of a shaken container of grains. We find that the peak velocity of the vibration, v max, controls the flux, i.e., the flux is nearly independent of the frequency and acceleration amplitude for a given value of v max. The flux decreases with increasing peak velocity and then becomes almost constant for the largest values of v max. The data at low peak velocity can be quantitatively described by a simple model, but the crossover to nearly constant flux at larger peak velocity suggests a regime in which the granular density near the container bottom is independent of the energy input to the system.


Nature | 2004

Getting to the bottom of a granular medium

Matthew Stone; David P. Bernstein; Rachel Barry; M. D. Pelc; Yee Kin Tsui; P. Schiffer

Penetration by an object through a dense granular medium (for example, by a finger pushing slowly into the sand on a beach) presents an interesting physics problem that is closely related to issues of practical importance in soil science. Here we measure the penetration-resistance force for an object approaching the solid bottom boundary of a granular sample — analogous to the finger approaching a flat rock buried in the beach. We find that the penetration resistance near the boundary increases exponentially, which demonstrates the existence of an intrinsic length scale to the ‘jamming’ caused by a locally applied stress.


PLOS ONE | 2017

Longitudinal multiparameter single-cell analysis of macaques immunized with pneumococcal protein-conjugated or unconjugated polysaccharide vaccines reveals distinct antigen specific memory B cell repertoires

Bin Jia; Lisa K. McNeil; Christopher D. Dupont; Konstantinos Tsioris; Rachel Barry; Ingrid L. Scully; Adebola O. Ogunniyi; Christopher Gonzalez; Michael W. Pride; Todd M. Gierahn; Paul Liberator; Kathrin U. Jansen; J. Christopher Love

Background The efficacy of protein-conjugated pneumococcal polysaccharide vaccines has been well characterized for children. The level of protection conferred by unconjugated polysaccharide vaccines remains less clear, particularly for elderly individuals who have had prior antigenic experience through immunization with unconjugated polysaccharide vaccines or natural exposure to Streptococcus pneumoniae. Methods We compared the magnitude, diversity and genetic biases of antigen-specific memory B cells in two groups of adult cynomolgus macaques that were immunized with a 7-valent conjugated vaccine and boosted after five years with either a 13-valent pneumococcal polysaccharide conjugate vaccine (13vPnC) or a 23-valent unconjugated pneumococcal polysaccharide vaccine (23vPS) using microengraving (a single-cell analysis method) and single-cell RT-PCR. Results Seven days after boosting, the mean frequency of antigen-specific memory B cells was significantly increased in macaques vaccinated with 13vPnC compared to those receiving 23vPS. The 13vPnC-vaccinated macaques also exhibited a more even distribution of antibody specificities to four polysaccharides in the vaccine (PS4, 6B, 14, 23F) that were examined. However, single-cell analysis of the antibody variable region sequences from antigen-specific B cells elicited by unconjugated and conjugated vaccines indicated that both the germline gene segments forming the heavy chains and the average lengths of the Complementary Determining Region 3 (CDR3) were similar. Conclusions Our results confirm that distinctive differences can manifest between antigen-specific memory B cell repertoires in nonhuman primates immunized with conjugated and unconjugated pneumococcal polysaccharide vaccines. The study also supports the notion that the conjugated vaccines have a favorable profile in terms of both the frequency and breadth of the anamnestic response among antigen-specific memory B cells.


Nature | 2004

Getting to the bottom of a granular medium: Stress propagation

Matthew Stone; David P. Bernstein; Rachel Barry; M. D. Pelc; Yee-Kin Tsui; P. Schiffer

Penetration by an object through a dense granular medium (for example, by a finger pushing slowly into the sand on a beach) presents an interesting physics problem that is closely related to issues of practical importance in soil science. Here we measure the penetration-resistance force for an object approaching the solid bottom boundary of a granular sample — analogous to the finger approaching a flat rock buried in the beach. We find that the penetration resistance near the boundary increases exponentially, which demonstrates the existence of an intrinsic length scale to the ‘jamming’ caused by a locally applied stress.


5th International Conference on the Micromechanics of Granular Media: Powders and Grains 2005 | 2005

Getting to the bottom and top of a granular medium

Matthew Stone; T. Scheidemantel; David P. Bernstein; Rachel Barry; M. D. Pelc; Y. K. Tsui; K. Klein; Ke Chen; P. Schiffer

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Matthew Stone

Oak Ridge National Laboratory

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David P. Bernstein

Pennsylvania State University

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M. D. Pelc

Pennsylvania State University

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K. Klein

Pennsylvania State University

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Ke Chen

Pennsylvania State University

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T. Scheidemantel

Pennsylvania State University

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Y. K. Tsui

Pennsylvania State University

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A. J. Morss

Pennsylvania State University

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Adebola O. Ogunniyi

Massachusetts Institute of Technology

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