Another expert system rule inference based on DNA molecule logic gates

With the help of silicon industry microfluidic processors were invented utilizing nano membrane valves, pumps and mi-croreactors. These so called lab-on-a-chips combined together with molecular computing create molecular-systems-on-a-chips. This work presents a new approach to implementation of molecular inference systems. It requires the unique representation of signals by DNA molecules. The main part of this work includes the concept of logic gates based on typical genetic engineering reactions. The presented method allows for constructing logic gates with many inputs and for executing them at the same quantity of elementary operations, regardless of a number of input signals. Every microreactor of the lab-on-a-chip performs one unique operation on input molecules and can be connected by dataflow output-input connections to other ones

Topics in Programming Languages, a Philosophical Analysis through the case of Prolog

[EN]Programming languages seldom find proper anchorage in philosophy of logic, language and science. is more, philosophy of language seems to be restricted to natural languages and linguistics, and even philosophy of logic is rarely framed into programming languages topics. The logic programming paradigm and Prolog are, thus, the most adequate paradigm and programming language to work on this subject, combining natural language processing and linguistics, logic programming and constriction methodology on both algorithms and procedures, on an overall philosophizing declarative status. Not only this, but the dimension of the Fifth Generation Computer system related to strong Al wherein Prolog took a major role. and its historical frame in the very crucial dialectic between procedural and declarative paradigms, structuralist and empiricist biases, serves, in exemplar form, to treat straight ahead philosophy of logic, language and science in the contemporaneous age as well. In recounting Prolog's philosophical, mechanical and algorithmic harbingers, the opportunity is open to various routes. We herein shall exemplify some: - the mechanical-computational background explored by Pascal, Leibniz, Boole, Jacquard, Babbage, Konrad Zuse, until reaching to the ACE (Alan Turing) and EDVAC (von Neumann), offering the backbone in computer architecture, and the work of Turing, Church, Gödel, Kleene, von Neumann, Shannon, and others on computability, in parallel lines, throughly studied in detail, permit us to interpret ahead the evolving realm of programming languages. The proper line from lambda-calculus, to the Algol-family, the declarative and procedural split with the C language and Prolog, and the ensuing branching and programming languages explosion and further delimitation, are thereupon inspected as to relate them with the proper syntax, semantics and philosophical élan of logic programming and Prolog

Modelos de computación lógica con ADN

La computación molecular es una disciplina que se ocupa del diseño e implementación de dispositivos para el procesamiento de información sobre un sustrato biológico, como el ácido desoxirribonucleico (ADN), el ácido ribonucleico (ARN) o las proteínas. Desde que Watson y Crick descubrieron en los años cincuenta la estructura molecular del ADN en forma de doble hélice, se desencadenaron otros descubrimientos como las enzimas que cortan el ADN o la reacción en cadena de la polimerasa (PCR), contribuyendo más que signi�cativamente a la irrupción de la tecnología del ADN recombinante. Gracias a esta tecnología y al descenso vertiginoso de los precios de secuenciación y síntesis del ADN, la computación biomolecular pudo abandonar su concepción puramente teórica. En 1994, Leonard Adleman logró resolver un problema de computación NP-completo (El Problema del Camino de Hamilton Dirigido) utilizando únicamente moléculas de ADN. La gran capacidad de procesamiento en paralelo ofrecida por las técnicas del ADN recombinante permitió a Adleman ser capaz de resolver dicho problema en tiempo polinómico, aunque a costa de un consumo exponencial de moléculas de ADN. Utilizando algoritmos similares al de �fuerza bruta� utilizado por Adleman se logró resolver otros problemas NP-completos (por ejemplo, el de Satisfacibilidad de Fórmulas Lógicas / SAT). Pronto se comprendió que la computación con biomolecular no podía competir en velocidad ni precisión con los ordenadores de silicio, por lo que su enfoque y objetivos se centraron en la resolución de problemas biológicos con aplicación biomédica, dejando de lado la resolución de problemas clásicos de computación. Desde entonces se han propuesto diversos modelos de dispositivos biomoleculares que, de forma autónoma (sin necesidad de un bio-ingeniero realizando operaciones de laboratorio), son capaces de procesar como entrada un sustrato biológico y proporcionar una salida también en formato biológico: procesadores que aprovechan la extensión de la Polimerasa, autómatas que funcionan con enzimas de restricción o con deoxiribozimas, circuitos de hibridación competitiva. Esta tesis presenta un conjunto de modelos de dispositivos de ácidos nucleicos escalables, sensibles al tiempo y energéticamente e�cientes, capaces de implementar diversas operaciones de computación lógica aprovechando el fenómeno de la hibridación competitiva del ADN. La capacidad implícita de estos dispositivos para aplicar reglas de inferencia como modus ponens, modus tollens, resolución o el silogismo hipotético tiene un gran potencial. Entre otras funciones, permiten representar implicaciones lógicas (o reglas del tipo SI/ENTONCES), como por ejemplo, �si se da el síntoma 1 y el síntoma 2, entonces estamos ante la enfermedad A�, o �si estamos ante la enfermedad B, entonces deben manifestarse los síntomas 2 y 3�. Utilizando estos módulos lógicos como bloques básicos de construcción, se pretende desarrollar sistemas in vitro basados en sensores de ADN, capaces de trabajar de manera conjunta para detectar un conjunto de síntomas de entrada y producir un diagnóstico de salida. La reciente publicación en la revista Science de un autómata biomolecular de diagnóstico, capaz de tratar las células cancerígenas sin afectar a las células sanas, es un buen ejemplo de la relevancia cientí�ca que este tipo de autómatas tienen en la actualidad. Además de las recién mencionadas aplicaciones en el diagnóstico in vitro, los modelos presentados también tienen utilidad en el diseño de biosensores inteligentes y la construcción de bases de datos con registros en formato biomolecular que faciliten el análisis genómico. El estudio sobre el estado de la cuestión en computación biomolecular que se presenta en esta tesis está basado en un artículo recientemente publicado en la revista Current Bioinformatics. Los nuevos dispositivos presentados en la tesis forman parte de una solicitud de patente de la que la UPM es titular, y han sido presentados en congresos internacionales como Unconventional Computation 2010 en Tokio o Synthetic Biology 2010 en París

A Formalization of Linkage Analysis

In this report a formalization of genetic linkage analysis is introduced. Linkage analysis is a computationally hard biomathematical method, which purpose is to locate genes on the human genome. It is rooted in the new area of bioinformatics and no formalization of the method has previously been established. Initially, the biological model is presented. On the basis of this biological model we establish a formalization that enables reasoning about algorithms used in linkage analysis. The formalization applies both for single and multi point linkage analysis. We illustrate the usage of the formalization in correctness proofs of central algorithms and optimisations for linkage analysis. A further use of the formalization is to reason about alternative methods for linkage analysis. We discuss the use of MTBDDs and PDGs in linkage analysis, since they have proven efficient for other computationally hard problems involving large state spaces. We conclude that none of the techniques discussed are directly applicable to linkage analysis, however further research is needed in order to investigated whether a modified version of one or more of these are applicable

A Formalization of Linkage Analysis

In this report a formalization of genetic linkage analysis is introduced. Linkage analysis is a computationally hard biomathematical method, which purpose is to locate genes on the human genome. It is rooted in the new area of bioinformatics and no formalization of the method has previously been established. Initially, the biological model is presented. On the basis of this biological model we establish a formalization that enables reasoning about algorithms used in linkage analysis. The formalization applies both for single and multi point linkage analysis. We illustrate the usage of the formalization in correctness proofs of central algorithms and optimisations for linkage analysis. A further use of the formalization is to reason about alternative methods for linkage analysis. We discuss the use of MTBDDs and PDGs in linkage analysis, since they have proven efficient for other computationally hard problems involving large state spaces. We conclude that none of the techniques discussed are directly applicable to linkage analysis, however further research is needed in order to investigated whether a modified version of one or more of these are applicable

Synthesising executable gene regulatory networks in haematopoiesis from single-cell gene expression data

A fundamental challenge in biology is to understand the complex gene regulatory networks which control tissue development in the mammalian embryo, and maintain homoeostasis in the adult. The cell fate decisions underlying these processes are ultimately made at the level of individual cells. Recent experimental advances in biology allow researchers to obtain gene expression profiles at single-cell resolution over thousands of cells at once. These single-cell measurements provide snapshots of the states of the cells that make up a tissue, instead of the population-level averages provided by conventional high-throughput experiments. The aim of this PhD was to investigate the possibility of using this new high resolution data to reconstruct mechanistic computational models of gene regulatory networks. In this thesis I introduce the idea of viewing single-cell gene expression profiles as states of an asynchronous Boolean network, and frame model inference as the problem of reconstructing a Boolean network from its state space. I then give a scalable algorithm to solve this synthesis problem. In order to achieve scalability, this algorithm works in a modular way, treating different aspects of a graph data structure separately before encoding the search for logical rules as Boolean satisfiability problems to be dispatched to a SAT solver. Together with experimental collaborators, I applied this method to understanding the process of early blood development in the embryo, which is poorly understood due to the small number of cells present at this stage. The emergence of blood from Flk1+ mesoderm was studied by single cell expression analysis of 3934 cells at four sequential developmental time points. A mechanistic model recapitulating blood development was reconstructed from this data set, which was consistent with known biology and the bifurcation of blood and endothelium. Several model predictions were validated experimentally, demonstrating that HoxB4 and Sox17 directly regulate the haematopoietic factor Erg, and that Sox7 blocks primitive erythroid development. A general-purpose graphical tool was then developed based on this algorithm, which can be used by biological researchers as new single-cell data sets become available. This tool can deploy computations to the cloud in order to scale up larger high-throughput data sets. The results in this thesis demonstrate that single-cell analysis of a developing organ coupled with computational approaches can reveal the gene regulatory networks that underpin organogenesis. Rapid technological advances in our ability to perform single-cell profiling suggest that my tool will be applicable to other organ systems and may inform the development of improved cellular programming strategies.Microsoft Research PhD Scholarshi