000 05609cam a2200601Mi 4500
001 ocn773564828
003 OCoLC
005 20171115112138.0
006 m o d
007 cr |n|---|||||
008 120123s2011 nju ob 000 0 eng d
020 _a9783527644582
_q(electronic bk.)
020 _a352764458X
_q(electronic bk.)
020 _a9783527644773
_q(electronic bk.)
020 _a3527644776
_q(electronic bk.)
029 1 _aAU@
_b000048852576
029 1 _aDEBSZ
_b431074321
029 1 _aNZ1
_b15922069
029 1 _aDEBBG
_bBV043394030
035 _a(OCoLC)773564828
_z(OCoLC)784138844
037 _a10.1002/9783527644582
_bWiley InterScience
_nhttp://www3.interscience.wiley.com
040 _aEBLCP
_beng
_epn
_cEBLCP
_dOCLCQ
_dUIU
_dN$T
_dDG1
_dYDXCP
_dOCLCQ
_dOHI
_dOCLCF
_dUKDOC
_dOCLCQ
_dDEBSZ
_dOCLCQ
049 _aMAIN
050 4 _aQP624.5.D726 .H889 2011
072 7 _aSCI
_x029000
_2bisacsh
082 0 4 _a572.8633
245 0 0 _aTag-based next generation sequencing /
_cedited by Matthias Harbers and Günter Kahl.
_h[electronic resource]
260 _aHoboken :
_bJohn Wiley & Sons,
_c2011.
300 _a1 online resource (609 pages)
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
505 0 _aTag-based Next Generation Sequencing; Contents; Preface; List of Contributors; Part One: Tag-Based Nucleic Acid Analysis; 1 DeepSuperSAGE: High-Throughput Transcriptome Sequencing with Now- and Next-Generation Sequencing Technologies; 1.1 Introduction; 1.2 Overview of the Protocols; 1.2.1 Principle of the SuperSAGE Method; 1.2.2 Power of the SuperSAGE Tag; 1.2.3 Development of DeepSuperSAGE; 1.2.4 Ditag-Based DeepSuperSAGE (for 454 Pyrosequencing); 1.2.5 Single-Tag-Based DeepSuperSAGE (HT-SuperSAGE); 1.3 Methods and Protocols; 1.3.1 Linker or Adapter Preparation; 1.3.2 RNA Samples.
505 8 _a1.3.3 cDNA Synthesis and NlaIII Digestion; 1.3.4 Tag Extraction from cDNA; 1.3.5 Tag Extraction from cDNA; 1.3.6 Purification of Linker-Tag Fragments; 1.3.7 Ditag or Adapter-Tag Formation and Amplification; 1.3.8 Preparation of Templates for Sequencing; 1.4 Applications; 1.4.1 Applications of DeepSuperSAGE in Combination with 454 Pyrosequencing; 1.4.2 Practical Analysis of HT-SuperSAGE; 1.5 Perspectives; References; 2 DeepCAGE: Genome-Wide Mapping of Transcription Start Sites; 2.1 Introduction; 2.2 What is CAGE?; 2.3 Why CAGE?; 2.4 Methods and Protocols; 2.4.1 Key Reagents and Consumables.
505 8 _a2.4.2 Precautions; 2.4.3 RNA Samples Used for DeepCAGE Library Preparation; 2.4.4 DeepCAGE Library Preparation; 2.5 Applications; 2.6 Perspectives; References; 3 Definition of Promotome-Transcriptome Architecture Using CAGEscan; 3.1 Introduction; 3.2 What is CAGEscan?; 3.3 Why CAGEscan?; 3.4 Methods and Protocols; 3.4.1 Key Reagents and Consumables; 3.4.2 Precautions; 3.4.3 RNA Samples Used for CAGEscan Library Preparation; 3.4.4 Considerations on Pooling CAGEscan Libraries; 3.4.5 CAGEscan Library Preparation; 3.5 Applications and Perspectives; References.
505 8 _a4 RACE: New Applications of an Old Method to Connect Exons; 4.1 Introduction; 4.2 Deep-RACE; 4.2.1 Choice of the Sequencer; 4.2.2 Validation of Promoter Studies; 4.2.3 Other Applications of Deep-RACE; 4.2.4 Limitations of Deep-RACE; 4.3 Methods Outline; 4.3.1 Primer Design; 4.3.2 Molecular Biology of Deep-RACE Library Preparation; 4.3.3 Sequencing of Deep-RACE Libraries; 4.3.4 Analysis; 4.4 Perspectives; References; 5 RNA-PET: Full-Length Transcript Analysis Using 5'- and 3'-Paired-End Tag Next-Generation Sequencing; 5.1 Introduction; 5.2 Methods and Protocols.
505 8 _a5.2.1 Key Reagents and Consumables; 5.2.2 Protocol; 5.3 Applications; 5.3.1 PET Sequencing with SOLiD; 5.3.2 Mapping of the PETs; 5.3.3 PET Clustering, Annotation, and Genome Browser Visualization; 5.4 Perspectives; References; 6 Stranded RNA-Seq: Strand-Specific Shotgun Sequencing of RNA; 6.1 Introduction; 6.1.1 Before Starting; 6.2 Methods and Protocols; 6.2.1 Preface; 6.2.2 Materials and Consumables; 6.2.3 Protocol; 6.3 Bioinformatic Considerations; 6.4 Applications; 6.5 Perspectives; References.
505 8 _a7 Differential RNA Sequencing (dRNA-Seq): Deep-Sequencing-Based Analysis of Primary Transcriptomes.
520 _aTag-based approaches were originally designed to increase the throughput of capillary sequencing, where concatemers of short sequences were first used in expression profiling. New Next Generation Sequencing methods largely extended the use of tag-based approaches as the tag lengths perfectly match with the short read length of highly parallel sequencing reactions. Tag-based approaches will maintain their important role in life and biomedical science, because longer read lengths are often not required to obtain meaningful data for many applications. Whereas genome re-sequencing and de novo sequ.
588 0 _aPrint version record.
650 0 _aDNA microarrays.
650 0 _aNeurobiology.
650 4 _aOligonucleotide array sequence analysis.
650 7 _aSCIENCE
_xLife Sciences
_xGenetics & Genomics.
_2bisacsh
650 7 _aDNA microarrays.
_2fast
_0(OCoLC)fst00886592
650 7 _aNeurobiology.
_2fast
_0(OCoLC)fst01036315
655 4 _aElectronic books.
700 1 _aHarbers, Matthias.
700 1 _aKahl, Günter.
776 0 8 _iPrint version:
_tTag-based Next Generation Sequencing.
_dHoboken : John Wiley & Sons, ©2011
_z9783527328192
856 4 0 _uhttp://onlinelibrary.wiley.com/book/10.1002/9783527644582
_zWiley Online Library
942 _2ddc
_cBK
999 _c205523
_d205523