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出版商:
Springer
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出版日期:
2025-06-25
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售價:
$7,090
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貴賓價:
9.5 折
$6,736
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語言:
英文
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頁數:
761
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裝訂:
Hardcover - also called cloth, retail trade, or trade
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ISBN:
3031862732
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ISBN-13:
9783031862731
商品描述
This book provides an introduction to computer-based methods for the analysis of genomic data. Breakthroughs in molecular and computational biology have contributed to the emergence of vast data sets, where millions of genetic markers for each individual are coupled with medical records, generating an unparalleled resource for linking human genetic variation to human biology and disease. Similar developments have taken place in animal and plant breeding, where genetic marker information is combined with production traits. An important task for the statistical geneticist is to adapt, construct and implement models that can extract information from these large-scale data. An initial step is to understand the methodology that underlies the probability models and to learn the modern computer-intensive methods required for fitting these models. The objective of this book, suitable for readers who wish to develop analytic skills to perform genomic research, is to provide guidance to take this first step. This book is addressed to numerate biologists who may lack the formal mathematical background of the professional statistician. For this reason, considerably more detailed explanations and derivations are offered. Examples are used profusely and a large proportion involves programming with the open-source package R. The code needed to solve the exercises is provided and it can be downloaded, allowing students to experiment by running the programs on their own computer. Part I presents methods of inference and computation that are appropriate for likelihood and Bayesian models. Part II discusses prediction for continuous and binary data using both frequentist and Bayesian approaches. Some of the models used for prediction are also used for gene discovery. The challenge is to find promising genes without incurring a large proportion of false positive results. Therefore, Part II includes a detour on the False Discovery Rate, assuming frequentist and Bayesian perspectives. The last chapter of Part II provides an overview of a selected number of non-parametric methods. Part III consists of exercises and their solutions. This second edition has benefited from many clarifications and extensions of themes discussed in the first edition. Daniel Sorensen holds PhD and DSc degrees from the University of Edinburgh and is an elected Fellow of the American Statistical Association. He was professor of Statistical Genetics at Aarhus University where, at present, he is professor emeritus.
商品描述(中文翻譯)
本書介紹了基於計算機的基因組數據分析方法。分子生物學和計算生物學的突破促成了龐大數據集的出現,每個個體的數百萬個遺傳標記與醫療記錄相結合,生成了一個無與倫比的資源,用於將人類遺傳變異與人類生物學和疾病聯繫起來。在動植物育種方面也發生了類似的發展,遺傳標記信息與生產性狀相結合。統計遺傳學家的重要任務是調整、構建和實施能夠從這些大規模數據中提取信息的模型。初步步驟是理解概率模型背後的方法論,並學習擬合這些模型所需的現代計算密集型方法。本書的目標是為希望發展分析技能以進行基因組研究的讀者提供指導,幫助他們邁出這第一步。
本書針對那些可能缺乏專業統計學家正式數學背景的生物學家。因此,提供了相當詳細的解釋和推導。書中大量使用示例,其中很大一部分涉及使用開源包 R 進行編程。解決練習所需的代碼已提供,並可下載,讓學生能夠在自己的計算機上運行程序進行實驗。
第一部分介紹了適用於似然和貝葉斯模型的推斷和計算方法。第二部分討論了使用頻率主義和貝葉斯方法對連續和二元數據的預測。一些用於預測的模型也用於基因發現。挑戰在於在不產生大量假陽性結果的情況下找到有前途的基因。因此,第二部分包括了對假發現率的繞道討論,假設頻率主義和貝葉斯的觀點。第二部分的最後一章提供了若干非參數方法的概述。第三部分由練習及其解答組成。本第二版受益於對第一版中討論主題的許多澄清和擴展。
丹尼爾·索倫森擁有愛丁堡大學的博士和科學博士學位,並被選為美國統計協會的會士。他曾是奧胡斯大學的統計遺傳學教授,目前是名譽教授。
作者簡介
Daniel Sorensen holds PhD and DSc degrees from the University of Edinburgh and is an elected Fellow of the American Statistical Association. He was professor of Statistical Genetics at Aarhus University where, at present, he is professor emeritus.
作者簡介(中文翻譯)
丹尼爾·索倫森擁有愛丁堡大學的博士(PhD)和科學博士(DSc)學位,並且是美國統計學會的當選會士。他曾擔任奧胡斯大學的統計遺傳學教授,目前是該校的名譽教授。