컨텐츠로 이동
Next generation sequencing in cancer research. Volume 1, Decoding the cancer genome 해당 항목을 미리보기
닫기해당 항목을 미리보기
확인중입니다…

Next generation sequencing in cancer research. Volume 1, Decoding the cancer genome

저자: Wei Wu; Hani Choudhry
출판사: New York, NY : Springer, 2013.
판/형식:   전자도서 : 문서 : 영어모든 판과 형식 보기
데이터베이스:WorldCat
요약:
Next Generation Sequencing (NGS) technology has placed important milestones in the life science and changed the direction in biomedical science inclucing cancer. Scientists around the world are attempting to find the root cause of cancer and they are looking for more direct and effective means to cure cancer. This journey to conquer cancer is more optimistic now with the unfolding of the cancer genome. This book  더 읽기…
평가:

(아무런 평가가 없습니다.) 0 리뷰와 함께 - 첫번째로 올려주세요.

주제
다음과 같습니다:

 

온라인으로 문서 찾기

이 항목에 대한 링크

도서관에서 사본 찾기

&AllPage.SpinnerRetrieving; 해당항목을 보유하고 있는 도서관을 찾는 중

상세정보

장르/형태: Electronic books
자료 유형: 문서, 인터넷 자료
문서 형식: 인터넷 자원, 컴퓨터 파일
모든 저자 / 참여자: Wei Wu; Hani Choudhry
ISBN: 9781461476450 1461476453 1461476445 9781461476443
OCLC 번호: 856631749
메모: Includes index.
설명: 1 online resource (xxiii, 383 pages) : illustrations
내용: Introduction: next generation sequencing technology and cancer research --
The majority of total nuclear-encoded non-ribosomal RNA in a human cell is dark matter unannotated RNA --
Total RNA-seq of breast cancer in hypoxia --
Altered antisense-to-sense transcript ratios in breast cancer --
Identification of piRNAs in Hela cells by massive parallel sequencing --
Discovery of new microRNAs by small RNAome deep sequencing in childhood acute lymphoblastic leukemia --
Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome --
Whole-exome sequencing in CIC and IDH1/2 contributing to human oligodendroglioma --
Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing --
Tumour evolution inferred by single-cell sequencing --
Characterization of the single-cell transcriptional landscape by highly multiplex RNA-seq --
Tracing the derivation of embryonic stem cells from the inner cell mass by single-cell RNASeq analysis --
Whole genome DNA methylation analysis based on high throughput sequencing technology --
Comparative methylome analysis of benign and malignant peripheral nerve sheath tumors --
High-resolution genome-wide mapping of HIF-binding sites by ChIP-seq --
MicroRNA transfection and AGO-bound CLIP-seq data sets reveal distinct determinants of miRNA action --
Genome-wide identification of polycomb-associated RNAs by RIP-seq --
Single-molecule sequencing: sequence methods to enable accurate quantisation --
Metabolic labeling of RNA uncovers principles of RNA production and degradation dynamics in mammalian cells --
Reprogramming transcription by distinct classes of enhancers functionally defined by eRNA --
The genome information process for cancer research: the challenge and perspective.
다른 제목 Decoding the cancer genome
책임: Wei Wu, Hani Choudhry, Editors.
더 많은 정보:

초록:

Next Generation Sequencing in Cancer Research  더 읽기…

리뷰

사용자-기여 리뷰
GoodReads 리뷰 가져오는 중…
DOGObooks 리뷰를 가지고 오는 중…

태그

첫번째 되기
요청하신 것을 확인하기

이 항목을 이미 요청하셨을 수도 있습니다. 만약 이 요청을 계속해서 진행하시려면 Ok을 선택하세요.

링크된 데이터


<http://www.worldcat.org/oclc/856631749>
library:oclcnum"856631749"
library:placeOfPublication
rdf:typeschema:MediaObject
rdf:typeschema:Book
rdf:valueUnknown value: dct
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:about
schema:alternateName"Decoding the cancer genome"
schema:bookFormatschema:EBook
schema:contributor
schema:contributor
schema:datePublished"2013"
schema:description"Introduction: next generation sequencing technology and cancer research -- The majority of total nuclear-encoded non-ribosomal RNA in a human cell is dark matter unannotated RNA -- Total RNA-seq of breast cancer in hypoxia -- Altered antisense-to-sense transcript ratios in breast cancer -- Identification of piRNAs in Hela cells by massive parallel sequencing -- Discovery of new microRNAs by small RNAome deep sequencing in childhood acute lymphoblastic leukemia -- Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome -- Whole-exome sequencing in CIC and IDH1/2 contributing to human oligodendroglioma -- Genetic and structural variation in the gastric cancer kinome revealed through targeted deep sequencing -- Tumour evolution inferred by single-cell sequencing -- Characterization of the single-cell transcriptional landscape by highly multiplex RNA-seq -- Tracing the derivation of embryonic stem cells from the inner cell mass by single-cell RNASeq analysis -- Whole genome DNA methylation analysis based on high throughput sequencing technology -- Comparative methylome analysis of benign and malignant peripheral nerve sheath tumors -- High-resolution genome-wide mapping of HIF-binding sites by ChIP-seq -- MicroRNA transfection and AGO-bound CLIP-seq data sets reveal distinct determinants of miRNA action -- Genome-wide identification of polycomb-associated RNAs by RIP-seq -- Single-molecule sequencing: sequence methods to enable accurate quantisation -- Metabolic labeling of RNA uncovers principles of RNA production and degradation dynamics in mammalian cells -- Reprogramming transcription by distinct classes of enhancers functionally defined by eRNA -- The genome information process for cancer research: the challenge and perspective."
schema:description"Next Generation Sequencing (NGS) technology has placed important milestones in the life science and changed the direction in biomedical science inclucing cancer. Scientists around the world are attempting to find the root cause of cancer and they are looking for more direct and effective means to cure cancer. This journey to conquer cancer is more optimistic now with the unfolding of the cancer genome. This book focuses on the application of various NGS in the frontier cancer genome research. The 18 chapters in this volume have been written by scientists with many outstanding contributions in their area and the join effort has created comprehensive insightful view on (1) Overview of next generation sequencing technology in cancer genome research (2) Genome regulation and targeted sequencing in cancer (3) RNA transcriptome (coding and non-coding) in cancer genome (4)The challenges of computational biology for cancer genome study. This book is a state-of-the-art reference to all scientific researchers and onologists who are interested in the understanding of the cancer initiatome at whole genome scale and to those are keen to translate the 'base pairs to bedside' for better management of cancer patients in the era of personalized medicine."
schema:exampleOfWork<http://worldcat.org/entity/work/id/1405305648>
schema:genre"Electronic books"
schema:inLanguage"en"
schema:name"Next generation sequencing in cancer research. Volume 1, Decoding the cancer genome"
schema:url<http://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&db=nlabk&AN=622876>
schema:url
schema:url<http://site.ebrary.com/id/10743870>
schema:url<http://lib.myilibrary.com?id=516885>
schema:workExample
schema:workExample
schema:workExample
wdrs:describedby

Content-negotiable representations

윈도우 닫기

WorldCat에 로그인 하십시오 

계정이 없으세요? 아주 간단한 절차를 통하여 무료 계정을 만드실 수 있습니다.