Edward Curry – författare

In biological research, the amount of data available to researchers has increased so much over recent years, it is becoming increasingly difficult to understand the current state of the art without some experience and understanding of data analytics and bioinformatics. An Introduction to Bioinformatics with R: A Practical Guide for Biologists leads the reader through the basics of computational analysis of data encountered in modern biological research. With no previous experience with statistics or programming required, readers will develop the ability to plan suitable analyses of biological datasets, and to use the R programming environment to perform these analyses. This is achieved through a series of case studies using R to answer research questions using molecular biology datasets. Broadly applicable statistical methods are explained, including linear and rank-based correlation, distance metrics and hierarchical clustering, hypothesis testing using linear regression, proportional hazards regression for survival data, and principal component analysis. These methods are then applied as appropriate throughout the case studies, illustrating how they can be used to answer research questions.

Key Features:

· Provides a practical course in computational data analysis suitable for students or researchers with no previous exposure to computer programming.

· Describes in detail the theoretical basis for statistical analysis techniques used throughout the textbook, from basic principles

· Presents walk-throughs of data analysis tasks using R and example datasets. All R commands are presented and explained in order to enable the reader to carry out these tasks themselves.

· Uses outputs from a large range of molecular biology platforms including DNA methylation and genotyping microarrays; RNA-seq, genome sequencing, ChIP-seq and bisulphite sequencing; and high-throughput phenotypic screens.

· Gives worked-out examples geared towards problems encountered in cancer research, which can also be applied across many areas of molecular biology and medical research.

This book has been developed over years of training biological scientists and clinicians to analyse the large datasets available in their cancer research projects. It is appropriate for use as a textbook or as a practical book for biological scientists looking to gain bioinformatics skills.

In biological research, the amount of data available to researchers has increased so much over recent years, it is becoming increasingly difficult to understand the current state of the art without some experience and understanding of data analytics and bioinformatics. An Introduction to Bioinformatics with R: A Practical Guide for Biologists leads the reader through the basics of computational analysis of data encountered in modern biological research. With no previous experience with statistics or programming required, readers will develop the ability to plan suitable analyses of biological datasets, and to use the R programming environment to perform these analyses. This is achieved through a series of case studies using R to answer research questions using molecular biology datasets. Broadly applicable statistical methods are explained, including linear and rank-based correlation, distance metrics and hierarchical clustering, hypothesis testing using linear regression, proportional hazards regression for survival data, and principal component analysis. These methods are then applied as appropriate throughout the case studies, illustrating how they can be used to answer research questions.

Key Features:

· Provides a practical course in computational data analysis suitable for students or researchers with no previous exposure to computer programming.

· Describes in detail the theoretical basis for statistical analysis techniques used throughout the textbook, from basic principles

· Presents walk-throughs of data analysis tasks using R and example datasets. All R commands are presented and explained in order to enable the reader to carry out these tasks themselves.

· Uses outputs from a large range of molecular biology platforms including DNA methylation and genotyping microarrays; RNA-seq, genome sequencing, ChIP-seq and bisulphite sequencing; and high-throughput phenotypic screens.

· Gives worked-out examples geared towards problems encountered in cancer research, which can also be applied across many areas of molecular biology and medical research.

This book has been developed over years of training biological scientists and clinicians to analyse the large datasets available in their cancer research projects. It is appropriate for use as a textbook or as a practical book for biological scientists looking to gain bioinformatics skills.

The three volume proceedings LNAI 11051 – 11053 constitutes the refereed proceedings of the European Conference on Machine Learning and Knowledge Discovery in Databases, ECML PKDD 2018, held in Dublin, Ireland, in September 2018. 

The contributions were organized in topical sections named as follows: Part I: adversarial learning; anomaly and outlier detection; applications; classification; clustering and unsupervised learning; deep learning; ensemble methods; and evaluation. Part II: graphs; kernel methods; learning paradigms; matrix and tensor analysis; online and active learning; pattern and sequence mining; probabilistic models and statistical methods; recommender systems; and transfer learning. Part III: ADS data science applications; ADS e-commerce;ADS engineering and design; ADS financial and security; ADS health; ADS sensing and positioning; nectar track; and demo track.

This two-volume set LNCS 15718-15719 constitutes the refereed proceedings of the 22nd European Semantic Web Conference, ESWC 2025, held in Portoroz, Slovenia, during June 1–5, 2025.The 45 full papers presented were carefully reviewed and selected from 155 submissions.The ESWC’s Research track addresses the theoretical, analytical, and empirical aspects of the semantic web, semantic technologies, knowledge graphs and semantics on the Web in general. The In-use track focuses on contributions that reuse and apply state-of-the-art semantic technologies or resources to real-world settings. The resource track deals with resource contributions that are, on the one hand innovative or novel, and on the other hand sharable and reusable (e.g. datasets, knowledge graphs, ontologies, workflows, benchmarks, frameworks), and provide the necessary scaffolding to support the generation of scientific work and advance the state of the art.

This two-volume set LNCS 15718-15719 constitutes the refereed proceedings of the 22nd European Semantic Web Conference, ESWC 2025, held in Portoroz, Slovenia, during June 1–5, 2025.The 45 full papers presented were carefully reviewed and selected from 155 submissions.The ESWC’s Research track addresses the theoretical, analytical, and empirical aspects of the semantic web, semantic technologies, knowledge graphs and semantics on the Web in general. The In-use track focuses on contributions that reuse and apply state-of-the-art semantic technologies or resources to real-world settings. The resource track deals with resource contributions that are, on the one hand innovative or novel, and on the other hand sharable and reusable (e.g. datasets, knowledge graphs, ontologies, workflows, benchmarks, frameworks), and provide the necessary scaffolding to support the generation of scientific work and advance the state of the art.