標(biāo)題: Titlebook: Algorithms for Next-Generation Sequencing Data; Techniques, Approach Mourad Elloumi Book 2017 Springer International Publishing AG 2017 Bio [打印本頁(yè)] 作者: Melanin 時(shí)間: 2025-3-21 19:29
書(shū)目名稱Algorithms for Next-Generation Sequencing Data影響因子(影響力)
書(shū)目名稱Algorithms for Next-Generation Sequencing Data影響因子(影響力)學(xué)科排名
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書(shū)目名稱Algorithms for Next-Generation Sequencing Data網(wǎng)絡(luò)公開(kāi)度學(xué)科排名
書(shū)目名稱Algorithms for Next-Generation Sequencing Data被引頻次
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書(shū)目名稱Algorithms for Next-Generation Sequencing Data讀者反饋
書(shū)目名稱Algorithms for Next-Generation Sequencing Data讀者反饋學(xué)科排名
作者: 尖牙 時(shí)間: 2025-3-21 22:36 作者: 教育學(xué) 時(shí)間: 2025-3-22 02:29
Algorithms for Indexing Highly Similar DNA Sequencesogies of high-throughput . (NGS). Hence, it is possible to sequence several genomes of organisms and a project (.) now provide about 2500 individual human genomes (sequences of more than three billion characters (A, C, G, T).作者: vector 時(shí)間: 2025-3-22 04:58
DNA-Seq Error Correction Based on Substring Indicess on NGS reads produced by genome sequencing of a clonal cell population, which has important applications like the de novo genome assembly of previously unknown genomes, for example, recently mutated parasites (Mellmann et al., PLoS ONE 6(7):e22751, 2011) or newly sequenced genomes (Locke et al., Nature 469:529–533, 2011).作者: Indict 時(shí)間: 2025-3-22 12:14
The Contig Assembly Problem and Its Algorithmic Solutionss some sequencing technology to output, for a given DNA fragment (not necessarily a whole genome), a collection of possibly overlapping sequences (called .) representing small parts of the initial DNA fragment. The second one aims at recovering the sequence of the entire DNA fragment by assembling the reads.作者: 斷言 時(shí)間: 2025-3-22 13:42 作者: 有發(fā)明天才 時(shí)間: 2025-3-22 19:53
Book 2017ts and technical information specifically on indexing, compression and storage; error correction; alignment; and assembly.?.The book will be of value to researchers, practitioners and students engaged with bioinformatics, computer science, mathematics, statistics and life sciences..作者: notice 時(shí)間: 2025-3-23 01:12
Notwendige rechtliche Voraussetzungen,This chapter deals with the compression of genomic data without reference genomes. It presents various techniques which have been specifically developed to compress sequencing data in lossless or lossy modes. The chapter also provides an evaluation of different NGS data compressor tools.作者: 食料 時(shí)間: 2025-3-23 03:43
De Novo NGS Data CompressionThis chapter deals with the compression of genomic data without reference genomes. It presents various techniques which have been specifically developed to compress sequencing data in lossless or lossy modes. The chapter also provides an evaluation of different NGS data compressor tools.作者: 光滑 時(shí)間: 2025-3-23 09:20
Der Verkauf notleidender Krediteogies of high-throughput . (NGS). Hence, it is possible to sequence several genomes of organisms and a project (.) now provide about 2500 individual human genomes (sequences of more than three billion characters (A, C, G, T).作者: endarterectomy 時(shí)間: 2025-3-23 10:49 作者: cluster 時(shí)間: 2025-3-23 16:24 作者: 不安 時(shí)間: 2025-3-23 21:32 作者: Antigen 時(shí)間: 2025-3-24 01:32 作者: Orchiectomy 時(shí)間: 2025-3-24 02:53 作者: 雄辯 時(shí)間: 2025-3-24 10:33
Der Verkauf von Non Performing Loansoption of . (NGS). There has been great progress in the development of a variety of different algorithms for different purposes. Researchers are now able to use sensitive and efficient alignment algorithms for a wide variety of applications, including genome-wide variation studies [1], quantitative 作者: Exuberance 時(shí)間: 2025-3-24 14:22
Die Bestimmung der Marktposition,have promoted the explosive growth of data volume. Unfortunately, the produced reads are short and prone to contain errors that are incurred during sequencing cycles. Both large data volume and sequencing errors have complicated the mapping of NGS reads onto the reference genome and have motivated t作者: 刺激 時(shí)間: 2025-3-24 17:26
Der Verkaufspreis in der Industriebiological sequences in the form of reads, i.e., short fragments of an organism’s genome. The advent of NGS poses new issues for computer scientists and bioinformaticians, leading to the design of algorithms for aligning and merging the reads in order to obtain an efficient and effective reconstruct作者: 嫻熟 時(shí)間: 2025-3-24 20:20
https://doi.org/10.1007/978-3-642-94468-0s some sequencing technology to output, for a given DNA fragment (not necessarily a whole genome), a collection of possibly overlapping sequences (called .) representing small parts of the initial DNA fragment. The second one aims at recovering the sequence of the entire DNA fragment by assembling t作者: 過(guò)分 時(shí)間: 2025-3-25 02:40
https://doi.org/10.1007/978-3-662-26401-0arch from traditional wet-lab work into a data- intensive analytical discipline (Koboldt et al., Cell 155(1):27–38, 2013). The . “sequencing by synthesis” technique (Mardis, Annu Rev Genomics Hum Genet 9:387–402, 2008) is one of the most popular and widely used NGS technologies.作者: 遺產(chǎn) 時(shí)間: 2025-3-25 03:30
https://doi.org/10.1007/978-3-662-26401-0ay been substituted by cheaper and more effective ones. At the same time, data processing evolved concurrently to face new challenges and problems posed by the new type of sequencing records. In this first section, we briefly outline how such an evolution of sequencing technologies developed and how作者: 大洪水 時(shí)間: 2025-3-25 11:09 作者: Fatten 時(shí)間: 2025-3-25 14:08 作者: plasma-cells 時(shí)間: 2025-3-25 18:54
Der Verkauf notleidender Krediteogies of high-throughput . (NGS). Hence, it is possible to sequence several genomes of organisms and a project (.) now provide about 2500 individual human genomes (sequences of more than three billion characters (A, C, G, T).作者: promote 時(shí)間: 2025-3-25 20:25
,Analyse der Durchführbarkeit eines MBO,s on NGS reads produced by genome sequencing of a clonal cell population, which has important applications like the de novo genome assembly of previously unknown genomes, for example, recently mutated parasites (Mellmann et al., PLoS ONE 6(7):e22751, 2011) or newly sequenced genomes (Locke et al., Nature 469:529–533, 2011).作者: 時(shí)代 時(shí)間: 2025-3-26 03:32
https://doi.org/10.1007/978-3-642-94468-0s some sequencing technology to output, for a given DNA fragment (not necessarily a whole genome), a collection of possibly overlapping sequences (called .) representing small parts of the initial DNA fragment. The second one aims at recovering the sequence of the entire DNA fragment by assembling the reads.作者: FACT 時(shí)間: 2025-3-26 06:09 作者: 慢慢沖刷 時(shí)間: 2025-3-26 11:09
Searching and Indexing Circular Patterns such structure (Grossi et al., Proceedings of algorithms in bioinformatics - 15th international workshop, WABI 2015, Atlanta, GA, Sept 10–12, 2015. Lecture notes in computer science, vol 9289, pp 203–216. Springer, Berlin, 2015; Gusfield, Algorithms on strings, trees, and sequences - computer scien作者: EWE 時(shí)間: 2025-3-26 13:03
Probabilistic Models for Error Correction of Nonuniform Sequencing Datalistic models. One common formulation is based on models over Hamming graphs. A particular focus will be on a more general formulation using hidden Markov models that can solve indel errors. These methods are suitable for the correction of reads from experiments with nonuniform coverage, like RNA-Se作者: OASIS 時(shí)間: 2025-3-26 20:05 作者: DAMP 時(shí)間: 2025-3-27 00:53 作者: Cougar 時(shí)間: 2025-3-27 01:55
Der Verkauf notleidender Kredite such structure (Grossi et al., Proceedings of algorithms in bioinformatics - 15th international workshop, WABI 2015, Atlanta, GA, Sept 10–12, 2015. Lecture notes in computer science, vol 9289, pp 203–216. Springer, Berlin, 2015; Gusfield, Algorithms on strings, trees, and sequences - computer scien作者: coalition 時(shí)間: 2025-3-27 06:15 作者: cochlea 時(shí)間: 2025-3-27 11:28
Der Verkauf von Non Performing Loansscovery [9], identification of causative mutations for rare genetic diseases [10–12], detection of chromosomal abnormalities in tumor genomes [13], and many other advances which similarly depend on rapid and cost-effective genome-wide sequencing.作者: 救護(hù)車 時(shí)間: 2025-3-27 13:53
Die Bestimmung der Marktposition,t only ungapped alignments or gapped alignments with very limited number of gaps (typically one gap), and thereby call for new aligners with fully gapped alignment supported. In this chapter, we present the CUSHAW software suite for NGS read alignment, which is open-source and consists of three indi作者: Nausea 時(shí)間: 2025-3-27 18:05
Der Verkaufspreis in der Industrieion of the genome. In this chapter, we focus on methods that can quickly and precisely establish whether two reads are similar or not and that allow to analyze biological sequences extracted with NGS technologies. In particular, the most widespread string-matching, alignment-based, and alignment-free algorithms are summarized and discussed.作者: bacteria 時(shí)間: 2025-3-27 23:40 作者: Harridan 時(shí)間: 2025-3-28 05:17 作者: harangue 時(shí)間: 2025-3-28 10:02 作者: 最小 時(shí)間: 2025-3-28 11:45
,Durchführung des Management Buy-Out,lation level measurement and the different algorithms that have been proposed to deal with it does not exist. Therefore, in this chapter all known WGBS error sources will be extensively reviewed and critically evaluated in order to suggest a couple of best practices to deal with all sources of bias in WGBS assays.作者: 脆弱吧 時(shí)間: 2025-3-28 15:46
Error Correction in Methylation Profiling From NGS Bisulfite Protocolslation level measurement and the different algorithms that have been proposed to deal with it does not exist. Therefore, in this chapter all known WGBS error sources will be extensively reviewed and critically evaluated in order to suggest a couple of best practices to deal with all sources of bias in WGBS assays.作者: nonsensical 時(shí)間: 2025-3-28 19:55
Book 2017ts and technical information specifically on indexing, compression and storage; error correction; alignment; and assembly.?.The book will be of value to researchers, practitioners and students engaged with bioinformatics, computer science, mathematics, statistics and life sciences..作者: ECG769 時(shí)間: 2025-3-29 01:38
String-Matching and Alignment Algorithms for Finding Motifs in NGS Dataion of the genome. In this chapter, we focus on methods that can quickly and precisely establish whether two reads are similar or not and that allow to analyze biological sequences extracted with NGS technologies. In particular, the most widespread string-matching, alignment-based, and alignment-free algorithms are summarized and discussed.作者: Adulterate 時(shí)間: 2025-3-29 05:41 作者: 小步走路 時(shí)間: 2025-3-29 10:56
Algorithms for Indexing Highly Similar DNA Sequencesogies of high-throughput . (NGS). Hence, it is possible to sequence several genomes of organisms and a project (.) now provide about 2500 individual human genomes (sequences of more than three billion characters (A, C, G, T).作者: antiquated 時(shí)間: 2025-3-29 15:12
Searching and Indexing Circular Patternscircular sequence comparison finds applications in several biological contexts (Barton et al., Experimental algorithms. Lecture notes in computer science, vol 9125, pp 247–258, 2015; Barton et al., Algorithms Mol Biol 9(9):2014; Uliel et al., Protein Eng 14(8):533–542, 2001). This motivates the desi作者: 自然環(huán)境 時(shí)間: 2025-3-29 16:47 作者: 東西 時(shí)間: 2025-3-29 21:40
Probabilistic Models for Error Correction of Nonuniform Sequencing Data for downstream applications. In this chapter, we discuss different formulations for sequencing read error corrections that are based on probabilistic models able to handle datasets with a nonuniform read coverage. Nonuniform coverage is common in several applications of NGS, including small RNA and作者: Congregate 時(shí)間: 2025-3-30 00:34
DNA-Seq Error Correction Based on Substring Indicess on NGS reads produced by genome sequencing of a clonal cell population, which has important applications like the de novo genome assembly of previously unknown genomes, for example, recently mutated parasites (Mellmann et al., PLoS ONE 6(7):e22751, 2011) or newly sequenced genomes (Locke et al., N
