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標(biāo)題: Titlebook: Applied Computational Genomics; Yin Yao Shugart Book 2012 Springer Science+Business Media Dordrecht 2012 Gene mapping.exon sequencing.link [打印本頁]

作者: 推翻    時間: 2025-3-21 19:53
書目名稱Applied Computational Genomics影響因子(影響力)




書目名稱Applied Computational Genomics影響因子(影響力)學(xué)科排名




書目名稱Applied Computational Genomics網(wǎng)絡(luò)公開度




書目名稱Applied Computational Genomics網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Applied Computational Genomics被引頻次




書目名稱Applied Computational Genomics被引頻次學(xué)科排名




書目名稱Applied Computational Genomics年度引用




書目名稱Applied Computational Genomics年度引用學(xué)科排名




書目名稱Applied Computational Genomics讀者反饋




書目名稱Applied Computational Genomics讀者反饋學(xué)科排名





作者: 彈藥    時間: 2025-3-21 22:49
Renewed Interest in Haplotype: From Genetic Marker to Gene Prediction,otype-based association analysis. In this chapter, we have introduced the concept of haplotype and its roles in genetic studies, have also documented the aspects of earlier method developments, have described some key methods and related software, and have discussed the renewed interest in recent ye
作者: 價值在貶值    時間: 2025-3-22 03:00

作者: Organonitrile    時間: 2025-3-22 08:10
2213-2775 licy makers, and graduate students majoring in biology, biostatistics, and bioinformatics. Dr. Yin Yao Shugart is investigator in the Intramural Research Program at the National Institute of Mental Health, Bethesda, Maryland USA. ? ? ? ? ? ? ? ? ? ? ? ? ?978-94-017-8063-6978-94-007-5558-1Series ISSN 2213-2775 Series E-ISSN 2213-2783
作者: 無能性    時間: 2025-3-22 10:46

作者: 最有利    時間: 2025-3-22 15:11
Idriss El-Thalji,Jayantha P. Liyanageotype-based association analysis. In this chapter, we have introduced the concept of haplotype and its roles in genetic studies, have also documented the aspects of earlier method developments, have described some key methods and related software, and have discussed the renewed interest in recent ye
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作者: 符合規(guī)定    時間: 2025-3-23 04:07

作者: Nutrient    時間: 2025-3-23 07:27
Peter W. Tse,Joseph Mathew,C.N. Koen the focus of genetic research shifted toward the study of the more complex common disorders, alternative approaches such as association studies were shown to be more successful in identifying common variants of small effect that are in part responsible for susceptibility to such conditions. Recen
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作者: dandruff    時間: 2025-3-24 11:46
https://doi.org/10.1007/978-3-030-48021-9challenge. The field of translational genomics is rapidly progressing with the development of next-generation sequencing (NGS) technologies. NGS is poised to produce a sea change in clinical practice by providing new insights into our understanding of complex human diseases. In this review, we will
作者: Crater    時間: 2025-3-24 17:03
Yin Yao ShugartProvides detailed introduction for the evolution of the field.Reviews statistical development and application in the area of human genomics.Describes the view of future direction towards translational
作者: 詞匯    時間: 2025-3-24 19:56

作者: 突變    時間: 2025-3-25 01:24
Introduction,rovides highlights for all nine chapters which have been collected in this book. The authors also list the critical concepts illustrated by the authors and point out logical connections between different chapters.
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作者: 重畫只能放棄    時間: 2025-3-25 10:31

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作者: oncologist    時間: 2025-3-25 17:05
Lecture Notes in Mechanical Engineeringrovides highlights for all nine chapters which have been collected in this book. The authors also list the critical concepts illustrated by the authors and point out logical connections between different chapters.
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作者: 上下連貫    時間: 2025-3-26 02:37

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作者: Dissonance    時間: 2025-3-26 10:24

作者: absolve    時間: 2025-3-26 13:39

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作者: 宿醉    時間: 2025-3-26 22:03

作者: Projection    時間: 2025-3-27 02:51

作者: Iatrogenic    時間: 2025-3-27 05:47
Plant Asset Management Today and Tomorrow,expression QTL and methylation QTL, presenting major findings and technique considerations, including experimental platform, sample quality, size, and heterogeneity, as well as analytical procedure and significance criteria. Lastly, we discussed the current and future use of QTL data in study of complex diseases.
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作者: Cloudburst    時間: 2025-3-27 23:36
Rare Variants Analysis in Unrelated Individuals,gions by collapsing or aggregating rare variants. To improve the statistical power, several weighting strategies to the rare variants and/or adding the informative covariates in the model have been published. In this chapter, some of these methods which can use unrelated individuals and family members are introduced.
作者: Expressly    時間: 2025-3-28 04:40

作者: 易于交談    時間: 2025-3-28 09:01
Gene Duplication and Functional Consequences,mechanisms may vary considerably in different organisms. In this chapter, we shall focus on a few important issues related to copy-number variation, gene essentiality, transcriptional, and epigenetic divergence between duplicate genes.
作者: pericardium    時間: 2025-3-28 13:26
Introduction,rovides highlights for all nine chapters which have been collected in this book. The authors also list the critical concepts illustrated by the authors and point out logical connections between different chapters.
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作者: ALLAY    時間: 2025-3-28 20:08

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作者: 怒目而視    時間: 2025-3-29 03:45
QTL Mapping of Molecular Traits for Studies of Human Complex Diseases,ine novel functional implications of genetic variants. Here we reviewed recent progress on QTL mapping of molecular traits, including gene expression, DNA methylation, as well as protein expression, metabolites. QTL mapping of molecular traits has better chance to succeed in relatively small sample
作者: SPECT    時間: 2025-3-29 11:16

作者: grudging    時間: 2025-3-29 15:17
Analytical Approaches for Exome Sequence Data,rlying Mendelian disease. It is possible that exome sequencing in a relatively small number of individuals showing ‘extreme’ phenotypes or more familial subtypes of complex disease may also be productive. Larger-scale exome and whole genome sequencing studies offer the potential to interrogate the c
作者: 完成    時間: 2025-3-29 15:37
Rare Variants Analysis in Unrelated Individuals,e genetic architecture of human diseases, their limitation of explaining the missing heritability motivated researchers to test the hypothesis that rare variants contribute to the variation of common diseases, that is, common disease/rare variants (CDRV) hypothesis. The fast developed high-throughpu
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作者: 浮雕寶石    時間: 2025-3-30 01:44





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