Bioinformatics for DNA Sequence Analysis 来自 Semantic Scholar 喜欢 0 阅读量: 153 作者: D Posada 摘要: The storage, processing, description, transmission, connection, and analysis of the waves of new genomic data have made bioinformatics skills essential for scientists working with DNA sequences....
Bioinformatics for DNA Sequence Analysis, pp. 65-91. Totowa (NJ): Humana Press.Jermiin LS, Ho JWK, Lau KW et al (2009) SeqVis: a tool for detecting compositional heterogeneity among aligned nucleotide s...
Supercomputing for the parallelization of whole genome analysis Abstract Motivation: The declining cost of generating DNA sequence is promoting an increase in whole genome sequencing, especially as applied to the human genome. Whole genome analysis requires the alignment and comparison of raw sequence dat...
Analysis pipelines for genomic sequencing data bioinformaticsrna-seqpipelinegenomicsanalysissequencingdnaatac-seqwgsilluminaweswgbsrrbsnyu UpdatedSep 30, 2024 Shell Bioinformatics analysis scripts, workflows, general code examples pythonbioinformaticsrgenomicsbiology ...
核糖体DNA (rDNA)编码核糖体RNA,是真核细胞不可缺少的成分。它有数百个拷贝,位于人类基因组5个近端着丝粒染色体上,其甲基化参与了多种重要的生理病理过程。rDNA的特殊重复结构和在基因组组装中的不良表现,导致人们对它甲基化模式的研究不...
“DNASTAR is my favorite tool for sequence analysis. My colleagues also love it.” Dr. Xin Yin, Sanford Burnham Prebys Medical Discovery Institute “Easy to use, intuitive interface makes working with sequences easy.” Matthew Nilles, University of North Dakota ...
Official git repository for Biopython (originally converted from CVS) python bioinformatics genomics protein-structure dna protein biopython phylogenetics sequence-alignment Updated Oct 28, 2024 Python google / deepvariant Star 3.2k Code Issues Pull requests DeepVariant is an analysis pipeline that ...
Finally, the downstream bioinformatics analysis for DNA sequence variants involves queries across multiple genomic databases to extract meaningful information about gene and variant nomenclature, variant prevalence, functional impact, and assertion of clinical significance. A user interface renders and visualize...
在本文中,作者提出了一种从生物序列(即 DNA、RNA 和蛋白质)中提取特征的整体工具。这些特征是预测输入序列的属性、结构或功能的机器学习模型的输入。作者的工具不仅支持 iLearnPlus 中的所有功能,还支持文献中存在的 30 个附加功能。而且,作者的工具基于 R 语言,它为生物信息学家将序列转换为特征向量提供了替代...
Precision-medicine approaches for chronic pain could help people to receive effective treatment from the start. James Mitchell Crow Article|25 September 2024 Intragenic DNA inversions expand bacterial coding capacity Reversible DNA inversions found entirely within genes enable increased coding capacity by ...